Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 2,101–2,200, newest first.
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2497-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2496-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2495-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2494-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2493-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2492-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2491-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2490-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2489-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2488-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2487-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2486-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2485-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2484-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2483-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2482-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2481-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2480-2026 · Official record ↗
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surfac…
Company / brand: Medline Industries recalls
Official ID Z-2479-2026 · Official record ↗
The near-infrared therapy device contains a lithium-ion battery that may malfunction, causing it to catch fire or burst into flames.
Company / brand: MITO RED LIGHT recalls
Official ID Z-2478-2026 · Official record ↗
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during tr…
Company / brand: GE Medical Systems recalls
Official ID Z-2477-2026 · Official record ↗
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during tr…
Company / brand: GE Medical Systems recalls
Official ID Z-2476-2026 · Official record ↗
GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during tr…
Company / brand: GE Medical Systems recalls
Official ID Z-2475-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2474-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2473-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2472-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2471-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2470-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2469-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2468-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2467-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2466-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2465-2026 · Official record ↗
Potential for overpressure alerts.
Company / brand: ConMed recalls
Official ID Z-2464-2026 · Official record ↗
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon…
Company / brand: Howmedica Osteonics recalls
Official ID Z-2462-2026 · Official record ↗
Stryker has identified that Triathlon Universal Baseplate Size 3 (lot UZD9IB), is contained in packaging labeled as Triathlon Universal Baseplate Size 4 (lot TYX7OB), and Triathlon…
Company / brand: Howmedica Osteonics recalls
Official ID Z-2461-2026 · Official record ↗
Assayed Whole blood control contains labeling with incorrect performance range.
Company / brand: Accriva Diagnostics recalls
Official ID Z-2460-2026 · Official record ↗
Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet end…
Company / brand: AMD Medicom recalls
Official ID Z-2459-2026 · Official record ↗
Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not consistently meet end…
Company / brand: AMD Medicom recalls
Official ID Z-2458-2026 · Official record ↗
Exposure to the low purge pressure occurrence may result in persistent low purge pressure alarms and, in some cases, interruption or loss of mechanical circulatory support.
Company / brand: Abiomed recalls
Official ID Z-2457-2026 · Official record ↗
Humeral nail due to a manufacturing error is missing distal holes and if implanted may lead to revision surgery but, if the missing holes are identified before implantation, an equ…
Company / brand: Smith & Nephew recalls
Official ID Z-2456-2026 · Official record ↗
Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.
Company / brand: Medtronic Navigation recalls
Official ID Z-2451-2026 · Official record ↗
The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
Company / brand: Steris recalls
Official ID Z-2450-2026 · Official record ↗
The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.
Company / brand: Steris recalls
Official ID Z-2449-2026 · Official record ↗
There is a potential for paint delamination (chipping/peeling) on the lighting system's light heads.
Company / brand: Steris recalls
Official ID Z-2448-2026 · 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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Official ID Z-2379-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.