1,617 recent medical device recalls in our current data. Showing 1,001–1,200, newest first.
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2447-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2446-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2445-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2444-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2443-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2442-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2441-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2440-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2439-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2438-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Centurion convenience kits recall status
Official ID Z-2437-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2436-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2435-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2434-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2433-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2432-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2431-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kit recall status
Official ID Z-2430-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kit recall status
Official ID Z-2429-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kit recall status
Official ID Z-2428-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kit recall status
Official ID Z-2427-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kit recall status
Official ID Z-2426-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kit recall status
Official ID Z-2425-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2424-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2423-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2422-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2421-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2420-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2419-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline convenience kits recall status
Official ID Z-2418-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G recall status
Official ID Z-2417-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: BLOCK TRAY DYNJRA2119A INDWELLING NERVE BLOCK DYNJRA1011A recall status
Official ID Z-2416-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716 recall status
Official ID Z-2415-2026 · Official record ↗
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Company / brand: Medline Industries recalls
Affected product: Medline EBSI Kit EBSI1534 recall status
Official ID Z-2414-2026 · Official record ↗
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Affected product: Philips Allura Xper with the following Model Numbers recall status
Official ID Z-2412-2026 · Official record ↗
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Affected product: Philips MultiDiagnost Eleva with the following Model Numbers recall status
Official ID Z-2411-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2397-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2396-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2395-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2394-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2393-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2392-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2391-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2390-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2389-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2388-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2387-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2386-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2385-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2384-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2383-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2382-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2381-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2380-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2379-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2378-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2377-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2376-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2375-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2374-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2373-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2372-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2371-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2370-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2369-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2368-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2367-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2366-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2365-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: Description/REF recall status
Official ID Z-2364-2026 · Official record ↗
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited repo…
Company / brand: ARROW INTERNATIONAL recalls
Affected product: PARACENTESIS KIT recall status
Official ID Z-2363-2026 · Official record ↗
Potential software error in the Automated Impella Controller ("AIC" ) when used in conjunction with left ventricular Impella devices.
Company / brand: Abiomed recalls
Affected product: Automated Impella Controller (AIC) recall status
Official ID Z-2360-2026 · Official record ↗
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration se…
Company / brand: Datex-Ohmeda recalls
Affected product: Panda Freestanding Warmer recall status
Official ID Z-2359-2026 · Official record ↗
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration se…
Company / brand: Datex-Ohmeda recalls
Affected product: Giraffe Warmer with Integrated Resuscitation System (iRes) recall status
Official ID Z-2358-2026 · Official record ↗
Blender knob shaft can loosen, which can affect the delivered oxygen concentration. The system can deliver an oxygen concentration that does not match the intended concentration se…
Company / brand: Datex-Ohmeda recalls
Affected product: Giraffe Stand-alone Infant Resuscitation System recall status
Official ID Z-2357-2026 · Official record ↗
Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the suction button …
Company / brand: Boston Scientific recalls
Affected product: Orca Single Use Air/Water and Suction Valves recall status
Official ID Z-2413-2026 · Official record ↗
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Company / brand: AVID Medical recalls
Affected product: Halyard recall status
Official ID Z-2410-2026 · Official record ↗
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Company / brand: AVID Medical recalls
Affected product: Halyard recall status
Official ID Z-2409-2026 · Official record ↗
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Company / brand: AVID Medical recalls
Affected product: Halyard recall status
Official ID Z-2408-2026 · Official record ↗
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Company / brand: AVID Medical recalls
Affected product: Halyard recall status
Official ID Z-2407-2026 · Official record ↗
Software may fail to load adapted baseline shift plan during treatment delivery when a communication error occurs.
Company / brand: Elekta recalls
Affected product: MOSAIQ Oncology Information System recall status
Official ID Z-2406-2026 · Official record ↗
Software malfunction may occur during pacing capture threshold test of pacemaker resulting in programmer not successfully communicating the command to terminate the test.
Company / brand: Abbott Medical recalls
Affected product: Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software recall status
Official ID Z-2405-2026 · Official record ↗
Sterile anchors my lack sterility assurance.
Company / brand: Boston Scientific Neuromodulation recalls
Affected product: Boston Scientific Model SC-4318 recall status
Official ID Z-2404-2026 · Official record ↗
Reusable electrodes may not meet expected performance levels.
Company / brand: Boston Scientific Neuromodulation recalls
Affected product: Boston Scientific TCN Electrodes recall status
Official ID Z-2403-2026 · Official record ↗
Reusable electrodes may not meet expected performance levels.
Company / brand: Boston Scientific Neuromodulation recalls
Affected product: Boston Scientific CSK Electrodes recall status
Official ID Z-2402-2026 · Official record ↗
There is an error in the labeling of the GTIN on the product. When scanned; however, the case labeling, lot number, and printed labeling on the product correctly identifies the pro…
Company / brand: Fresenius Medical Care Holdings recalls
Affected product: Bicarby Dialysate recall status
Official ID Z-2401-2026 · Official record ↗
Some units of Aluminum Chloride Gel contain the package insert for Ferric Sulfate Gel. The incorrect insert misidentifies the product and contains different first aid instructions,…
Company / brand: Inter-Med recalls
Affected product: Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit recall status
Official ID Z-2400-2026 · Official record ↗
Through customer complaints, the ankle replacement system was found to contain incorrect devices: Left implant packaging and labeling bears a right implant device.
Company / brand: DT MedTech recalls
Affected product: Hintermann Series Talar Implant recall status
Official ID Z-2399-2026 · Official record ↗
A potential positive bias in quality control (QC) and patient sample results in three lots of the Dimension Tacrolimus (TAC) Flex reagent cartridge.
Company / brand: Siemens Healthcare Diagnostics recalls
Affected product: Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC) recall status
Official ID Z-2398-2026 · Official record ↗
It was reported that plates 2 and 3 were marked as passed , although it appeared that QC had not been performed on these plates, despite samples being measured. The potential clini…
Company / brand: The Binding Site Group recalls
Affected product: Brand Name recall status
Official ID Z-2362-2026 · Official record ↗
The cannulation of the CCS screw is not centered.
Company / brand: Medartis AG recalls
Affected product: Medartis APTUS recall status
Official ID Z-2361-2026 · Official record ↗
Yttrium-stabilized zirconium oxide discs for fixed all-ceramic dental restorations may have reduced or missing dentin layer and when used clinically in the patient's mouth there is…
Company / brand: Sagemax Bioceramics recalls
Affected product: NexxZr T Multi A3 recall status
Official ID Z-2356-2026 · Official record ↗
Due to the Magnetic Resonance Conditional Symbol missing on the carton, inner tray, and patient label.
Company / brand: In2bones USA recalls
Affected product: NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 recall status
Official ID Z-2355-2026 · Official record ↗
System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.
Company / brand: Philips North America recalls
Affected product: DigitalDiagnost C90 Flex/Value/Chest/ER recall status
Official ID Z-2354-2026 · Official record ↗
Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple amplifier configuratio…
Company / brand: Micromed S.p.A recalls
Affected product: SD LTM 64 PLUS recall status
Official ID Z-2353-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2352-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2351-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2350-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2349-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2348-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2347-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2346-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2345-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2344-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2343-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2342-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2341-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2340-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2339-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2338-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2337-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2336-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Product Name recall status
Official ID Z-2335-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Brand Name recall status
Official ID Z-2334-2026 · Official record ↗
Lidocaine hydrochloride injection, the subject of a supplier recall for quality issues, were included into sterile kits and sets.
Company / brand: Avanos Medical recalls
Affected product: Brand Name recall status
Official ID Z-2333-2026 · Official record ↗
Due to incorrect incubation process being performed on product.
Company / brand: HF Acquisition Co recalls
Affected product: Brand Name recall status
Official ID Z-2332-2026 · Official record ↗
Due to incorrect incubation process being performed on product.
Company / brand: HF Acquisition Co recalls
Affected product: Brand Name recall status
Official ID Z-2331-2026 · Official record ↗
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Affected product: CGuard¿ Prime Carotid Stent System recall status
Official ID Z-2330-2026 · Official record ↗
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Affected product: CGuard Prime Carotid Stent System recall status
Official ID Z-2329-2026 · Official record ↗
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Affected product: Brand Name recall status
Official ID Z-2328-2026 · Official record ↗
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Affected product: CGuard Prime Carotid Stent System recall status
Official ID Z-2327-2026 · Official record ↗
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Affected product: Brand Name recall status
Official ID Z-2326-2026 · Official record ↗
Stent delivery system may encounter complications during deployment which may result in high resistance or inability to deploy the stent.
Company / brand: INSPIREMD recalls
Affected product: Brand Name recall status
Official ID Z-2325-2026 · Official record ↗
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Company / brand: D.O.R.C. Dutch Opthalmic Research Center Intl B.V recalls
Affected product: TDC VELOCE" recall status
Official ID Z-2324-2026 · Official record ↗
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Company / brand: D.O.R.C. Dutch Opthalmic Research Center Intl B.V recalls
Affected product: TDC VELOCE" recall status
Official ID Z-2323-2026 · Official record ↗
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Company / brand: D.O.R.C. Dutch Opthalmic Research Center Intl B.V recalls
Affected product: TDC VELOCE" recall status
Official ID Z-2322-2026 · Official record ↗
Given the increased number of leaks reported by users, it was determined to be the appropriate course of action to notify users of the potential for the occurrence of Bicarby luer-…
Company / brand: Fresenius Medical Care Holdings recalls
Affected product: Bicarby" Dialysate recall status
Official ID Z-2321-2026 · Official record ↗
Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures.
Company / brand: BERLIN HEART recalls
Affected product: EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves recall status
Official ID Z-2320-2026 · Official record ↗
The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.
Company / brand: Mozarc Medical US recalls
Affected product: Mahurkar Elite PASS Trays recall status
Official ID Z-2319-2026 · Official record ↗
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…
Company / brand: GE Medical Systems recalls
Affected product: Allia Moveo angiographic X-ray system recall status
Official ID Z-2318-2026 · Official record ↗
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…
Company / brand: GE Medical Systems recalls
Affected product: Allia IGS Pulse angiographic X-ray system recall status
Official ID Z-2317-2026 · Official record ↗
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…
Company / brand: GE Medical Systems recalls
Affected product: Allia IGS 7 Pulse angiographic X-ray system recall status
Official ID Z-2316-2026 · Official record ↗
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…
Company / brand: GE Medical Systems recalls
Affected product: Allia IGS 5 Pulse angiographic X-ray system recall status
Official ID Z-2315-2026 · Official record ↗
GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead to a risk of electrica…
Company / brand: GE Medical Systems recalls
Affected product: Allia IGS 3 Pulse angiographic X-ray system recall status
Official ID Z-2314-2026 · Official record ↗
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…
Company / brand: ICU Medical recalls
Affected product: Plum Duo Precision IV Pump recall status
Official ID Z-2313-2026 · Official record ↗
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…
Company / brand: ICU Medical recalls
Affected product: Plum Duo Infusion Pump recall status
Official ID Z-2312-2026 · Official record ↗
Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may…
Company / brand: ICU Medical recalls
Affected product: Plum Solo Precision IV Pump recall status
Official ID Z-2311-2026 · Official record ↗
A defect has been identified in the manufacture of the Fresh Roast Systems ColorTrack instrument model number BENCH R-100 which could under very rare specific misuse circumstances …
Company / brand: Fresh Roast Systems recalls
Affected product: Fresh Roast Systems ColorTrack recall status
Official ID Z-2280-2026 · Official record ↗
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching fro…
Company / brand: Intuitive Surgical recalls
Affected product: Brand Name recall status
Official ID Z-2310-2026 · Official record ↗
3.0mm surgical knives labeled and packaged as 2.2mm surgical knives.
Company / brand: SSC- Surgical Specialties recalls
Affected product: Sharpoint 2 recall status
Official ID Z-2309-2026 · Official record ↗
Due to incorrect functional length on device labeling.
Company / brand: Grace Medical recalls
Affected product: TITANIUM/FLUOROPLASTIC PISTON 0 recall status
Official ID Z-2308-2026 · Official record ↗
Lidocaine Hydrochloride Injection, USP, which was recalled by a supplier for quality issues, was included in custom convenience kits.
Company / brand: Windstone Medical Packaging recalls
Affected product: Aligned Medical AMS16835 Fluids Kit RX recall status
Official ID Z-2307-2026 · Official record ↗
Software in development inadvertently made available for customer use. Use of this software version can result in clinical information being associated with the incorrect patient. …
Company / brand: GE Medical Systems China Co recalls
Affected product: MAC 5 A4 Resting ECG Analysis System 855001-001 recall status
Official ID Z-2306-2026 · Official record ↗
Sterile wound dressing, lacks sterility assurance
Company / brand: DeRoyal Industries recalls
Affected product: DeRoyal Industries Inc recall status
Official ID Z-2305-2026 · Official record ↗
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Affected product: BD Pyxis MedBank Mini REF recall status
Official ID Z-2304-2026 · Official record ↗
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Affected product: BD Pyxis MedBank Tower REF recall status
Official ID Z-2303-2026 · Official record ↗
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Affected product: BD Pyxis MedStation ES Tower REF recall status
Official ID Z-2302-2026 · Official record ↗
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Affected product: BD Pyxis Mini Main REF recall status
Official ID Z-2301-2026 · Official record ↗
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Affected product: BD Pyxis Anesthesia Station 4000 REF recall status
Official ID Z-2300-2026 · Official record ↗
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Affected product: BD Pyxis Anesthesia Station ES REF recall status
Official ID Z-2299-2026 · Official record ↗
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Affected product: BD Pyxis MedStation ES REF recall status
Official ID Z-2298-2026 · Official record ↗
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Company / brand: CareFusion 303 recalls
Affected product: BD Pyxis MedStation 4000 REF recall status
Official ID Z-2297-2026 · Official record ↗
Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock c…
Company / brand: Bayer Medical Care recalls
Affected product: Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the M recall status
Official ID Z-2296-2026 · Official record ↗
Some of the Calibration/Output Certificates had the outputs reversed.
Company / brand: Daavlin Distributing Company recalls
Affected product: Phothera 200 recall status
Official ID Z-2295-2026 · Official record ↗
Electromagnetic contactors within high voltage generator may weld together, resulting in current being supplied to power supply even if power is off.
Company / brand: Shimadzu Medical Systems recalls
Affected product: Digital Angiography System Trinias recall status
Official ID Z-2294-2026 · Official record ↗
The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
Company / brand: Kico Knee Innovation Company recalls
Affected product: Arvis Hip & Knee 2 recall status
Official ID Z-2293-2026 · Official record ↗
The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
Company / brand: Kico Knee Innovation Company recalls
Affected product: Arvis Hip & Knee 3 recall status
Official ID Z-2292-2026 · Official record ↗
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Affected product: Philips Azurion 7M20 recall status
Official ID Z-2291-2026 · Official record ↗
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Affected product: Philips Azurion 7M12 recall status
Official ID Z-2290-2026 · Official record ↗
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Affected product: Philips Azurion 7B20/15 recall status
Official ID Z-2289-2026 · Official record ↗
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Affected product: Philips Azurion 7B12/12 recall status
Official ID Z-2288-2026 · Official record ↗
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Affected product: Philips Azurion 5M20 recall status
Official ID Z-2287-2026 · Official record ↗
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Affected product: Philips Azurion 5M12 recall status
Official ID Z-2286-2026 · Official record ↗
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Affected product: Philips Azurion 3M15 recall status
Official ID Z-2285-2026 · Official record ↗
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly tou…
Company / brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V recalls
Affected product: Philips Azurion 3M12 recall status
Official ID Z-2284-2026 · Official record ↗
Due to incorrect shelf-life expiration date.
Company / brand: Advanced Bionics recalls
Affected product: Brand Name recall status
Official ID Z-2283-2026 · Official record ↗
It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being ship…
Company / brand: Stryker recalls
Affected product: Neptune Smart Docking Station (120V) recall status
Official ID Z-2282-2026 · Official record ↗
The presence of holes in the pouch may compromise the package s ability to maintain the sterile barrier and protect the product from environmental exposure.
Company / brand: Covidien recalls
Affected product: Covidien EndoStitch" Polysorb Single Use Loading Unit recall status
Official ID Z-2281-2026 · Official record ↗
Electrical sparking may occur at the printer head. If the Electrostatic Discharge (ESD) printer brush becomes dislodged, electrical sparking at the printer head can result in charr…
Company / brand: GE Medical Systems Information Technologies recalls
Affected product: CASE v7 recall status
Official ID Z-2279-2026 · Official record ↗
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti…
Company / brand: B Braun Medical recalls
Affected product: Design Options Spinal Tray Spinal Needle Anesthesia procedure kits recall status
Official ID Z-2278-2026 · Official record ↗
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti…
Company / brand: B Braun Medical recalls
Affected product: Spinocan Spinal Needle procedure kits recall status
Official ID Z-2277-2026 · Official record ↗
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huons Co, Ltd., has issued a voluntary recall due to potenti…
Company / brand: B Braun Medical recalls
Affected product: Spinal Needle procedure kits recall status
Official ID Z-2276-2026 · Official record ↗
The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the produc…
Company / brand: Oculus Technologies of Mexico recalls
Affected product: PhaseOne Antimicrobial Solution recall status
Official ID Z-2275-2026 · Official record ↗
Potential for the Cassette Loading Lever to break.
Company / brand: Fresenius Kabi USA recalls
Affected product: The Large Volume Pump (LVP) of the Ivenix Infusion System (IIS) recall status
Official ID Z-2274-2026 · Official record ↗
Temperature probe devices lack FDA clearance.
Company / brand: Covidien recalls
Affected product: Covidien Mon-a-Therm general purpose temperature probe size recall status
Official ID Z-2273-2026 · Official record ↗
Temperature probe devices lack FDA clearance.
Company / brand: Covidien recalls
Affected product: Covidien Mon-a-Therm General Purpose Temperature Probe REF recall status
Official ID Z-2272-2026 · Official record ↗
Temperature probe devices lack FDA clearance.
Company / brand: Covidien recalls
Affected product: Covidien Mon-a-Therm Esophageal Stethoscope with Temperature Sensor 400TM REF recall status
Official ID Z-2271-2026 · Official record ↗
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Affected product: Brand Name recall status
Official ID Z-2270-2026 · Official record ↗
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Affected product: Brand Name recall status
Official ID Z-2269-2026 · Official record ↗
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Affected product: Brand Name recall status
Official ID Z-2268-2026 · Official record ↗
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Affected product: Brand Name recall status
Official ID Z-2267-2026 · Official record ↗
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Affected product: Brand Name recall status
Official ID Z-2266-2026 · Official record ↗
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Affected product: Brand Name recall status
Official ID Z-2265-2026 · Official record ↗
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Affected product: Brand Name recall status
Official ID Z-2264-2026 · Official record ↗
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential crackin…
Company / brand: B Braun Medical recalls
Affected product: Brand Name recall status
Official ID Z-2263-2026 · Official record ↗
Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow efficiency, incomplete or slow…
Company / brand: Baxter Healthcare recalls
Affected product: Brand Name recall status
Official ID Z-2262-2026 · Official record ↗
Due to customer complaint regarding incorrect display box labeling.
Company / brand: Covidien recalls
Affected product: COVIDIEN Shiley Tracheostomy Tube Cuffed with Inner Cannula REF 6FEN UDI-DI code recall status
Official ID Z-2261-2026 · Official record ↗
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Affected product: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall status
Official ID Z-2257-2026 · Official record ↗
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Affected product: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall status
Official ID Z-2256-2026 · Official record ↗
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Affected product: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall status
Official ID Z-2255-2026 · Official record ↗
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Affected product: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall status
Official ID Z-2254-2026 · Official record ↗
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Affected product: BD¿Spinal Tray with BD¿Whitacre Needle 25 G x 3 recall status
Official ID Z-2253-2026 · Official record ↗
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Affected product: BD¿Spinal Tray with BD¿Whitacre Needle 24 G x 3 recall status
Official ID Z-2252-2026 · Official record ↗
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Affected product: BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3 recall status
Official ID Z-2251-2026 · Official record ↗
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Affected product: BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3 recall status
Official ID Z-2250-2026 · Official record ↗
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Affected product: BD¿Spinal Tray with BD¿Quincke Needle 25 G x 3 recall status
Official ID Z-2249-2026 · Official record ↗
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identifi…
Company / brand: Becton Dickinson & Company recalls
Affected product: BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3 recall status
Official ID Z-2248-2026 · Official record ↗
Fresenius Kabi has been made aware via customer complaints that dropping or severe jarring of the Ivenix LVP may cause damage to internal components that may not be apparent or rea…
Company / brand: Fresenius Kabi USA recalls
Affected product: Ivenix Infusion System (IIS) recall status
Official ID Z-2224-2026 · Official record ↗
Potential software anomaly that can cause the pump to report a false battery-health value (typically 69%) and trigger a battery-depletion alarm that will shut down the pump unless …
Company / brand: Fresenius Kabi USA recalls
Affected product: LVP software of the Ivenix Infusion System (IIS) recall status
Official ID Z-2223-2026 · Official record ↗
If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended, there is an increased ris…
Company / brand: KAYSERBETTEN & CO. KG recalls
Affected product: Pediatric care bed recall status
Official ID Z-2212-2026 · Official record ↗
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Sources last checked October 22, 2026 at 12:00 PM UTC.