Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 2,201–2,300, newest first.
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-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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
Official ID Z-2357-2026 · Official record ↗
Undeclared melatonin.
Company / brand: Dkiru recalls
Official ID H-1079-2026 · Official record ↗
Potential for Salmonella
Company / brand: International Food Products recalls
Official ID H-1078-2026 · Official record ↗
Potential for Salmonella
Company / brand: International Food Products recalls
Official ID H-1077-2026 · Official record ↗
Product tested positive for Salmonella
Company / brand: International Food Products recalls
Official ID H-1076-2026 · Official record ↗
Undeclared fish.
Company / brand: Azuma Foods International USA recalls
Official ID H-1075-2026 · Official record ↗
Products were made with recalled California Dairies milk powder due to Salmonella.
Company / brand: Jonco Industries recalls
Official ID H-0953-2026 · Official record ↗
Plain salt was labeled as iodized and iodized salt was labeled as plain.
Company / brand: United Salt recalls
Official ID H-0952-2026 · Official record ↗
Product requires refrigeration but the label is missing a "Keep Refrigerated" statement
Company / brand: Fairhope Roasting Company recalls
Official ID H-0951-2026 · Official record ↗
Product may be contaminated with Salmonella
Company / brand: GREENWORLD FOOD EXPRESS (USA) recalls
Official ID H-0950-2026 · Official record ↗
Firm observed oily and sticky substance on direct food contact surface packaging of finished product.
Company / brand: United States Bakery recalls
Official ID H-0949-2026 · Official record ↗
Undeclared Allergen (Soy)
Company / brand: Nutrisystem recalls
Official ID H-0947-2026 · Official record ↗
The product contains unapproved colors chlorophyll E140 and E141.
Company / brand: MID DOLCIARIA SRL recalls
Official ID H-0946-2026 · Official record ↗
The product contains unapproved colors chlorophyll E140 and E141.
Company / brand: MID DOLCIARIA SRL recalls
Official ID H-0945-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0642-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0641-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0640-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0639-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0638-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0637-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0636-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0635-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0634-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0633-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0632-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0631-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0630-2026 · Official record ↗
CGMP Deviations; deficiencies observed during FDA inspection
Company / brand: Dabur India recalls
Official ID D-0629-2026 · Official record ↗
Failed Dissolution Specifications
Company / brand: Inventia Healthcare recalls
Official ID D-0610-2026 · Official record ↗
Labeling: Incorrect or Missing Lot and/or Exp Date
Company / brand: Sandoz recalls
Official ID D-0608-2026 · Official record ↗
Defective container:may contain bottles with incomplete seals
Company / brand: Keystone Industries recalls
Official ID D-0606-2026 · Official record ↗
Defective container:may contain bottles with incomplete seals
Company / brand: Keystone Industries recalls
Official ID D-0605-2026 · Official record ↗
Defective container:may contain bottles with incomplete seals
Company / brand: Keystone Industries recalls
Official ID D-0604-2026 · Official record ↗
Defective container:may contain bottles with incomplete seals
Company / brand: Keystone Industries recalls
Official ID D-0603-2026 · Official record ↗
Defective container:may contain bottles with incomplete seals
Company / brand: Keystone Industries recalls
Official ID D-0602-2026 · Official record ↗
Defective container:may contain bottles with incomplete seals
Company / brand: Keystone Industries recalls
Official ID D-0601-2026 · Official record ↗
Defective container:may contain bottles with incomplete seals
Company / brand: Keystone Industries recalls
Official ID D-0600-2026 · Official record ↗
Crystallization; identified as Buprenorphine free base
Company / brand: Par Health USA recalls
Official ID D-0596-2026 · Official record ↗
Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
Company / brand: Ajanta Pharma USA recalls
Official ID D-0594-2026 · Official record ↗
Subpotent Drug
Company / brand: IntegraDose Compounding Services recalls
Official ID D-0593-2026 · Official record ↗
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
Company / brand: PAI Holdings recalls
Official ID D-0592-2026 · Official record ↗
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
Company / brand: PAI Holdings recalls
Official ID D-0591-2026 · Official record ↗
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
Company / brand: PAI Holdings recalls
Official ID D-0590-2026 · Official record ↗
Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
Company / brand: PAI Holdings recalls
Official ID D-0589-2026 · Official record ↗
Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.
Company / brand: Glenmark Pharmaceuticals recalls
Official ID D-0588-2026 · Official record ↗
A loose nut that separates from the steering gear assembly while driving can cause a loss of steering control, increasing the risk of a crash.
Company / brand: General Motors recalls
Official ID 26V399000 · Official record ↗
A wheelchair lift that continues to move while occupied increases the risk of injury.
Company / brand: Ricon recalls
Official ID 26E038000 · Official record ↗
Inadequate protection may increase the risk of a fire.
Company / brand: Rockford recalls
Official ID 26E037000 · Official record ↗
Electrical shock increases the risk of injury.
Company / brand: Forest River recalls
Official ID 26V398000 · Official record ↗
Incorrect wheel rim size information could lead to improperly mounted tires and result in a loss of motorcycle control, increasing the risk of a crash.
Company / brand: Indian Motorcycle Company recalls
Official ID 26V397000 · Official record ↗
An overheated printed circuit board increases the risk of a fire.
Company / brand: Airxcel recalls
Official ID 26E036000 · Official record ↗
Loss of lighting can reduce visibility, increasing the risk of a crash.
Company / brand: Piaggio Group Americas recalls
Official ID 26V396000 · Official record ↗
A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing …
Company / brand: Farber Specialty Vehicles recalls
Official ID 26V395000 · Official record ↗
A person, especially a child, may be trapped by a rear powered seatback, increasing their risk of injury.
Company / brand: General Motors recalls
Official ID 26V394000 · Official record ↗
An unexpected loss of drive power increases the risk of a crash.
Company / brand: Toyota Motor Engineering & Manufacturing recalls
Official ID 26V393000 · Official record ↗
The baby loungers violate the mandatory standard for Infant Sleep Products because the sides are shorter than the minimum side height limit to secure the infant; the sleeping pad's…
Company / brand: CooCooBaby recalls
Official ID 26569 · Official notice ↗
The recalled car seat adapters can fail to properly attach to the stroller, which may allow the car seat to fall, posing a risk of serious injury from a fall hazard.
Company / brand: Joolz USA recalls
Official ID 26568 · Official notice ↗
The recalled children’s pajamas violate the mandatory flammability standard for children’s sleepwear, posing a risk of serious burn injuries or death.
Company / brand: SHEIN Distribution recalls
Official ID 26567 · Official notice ↗
The recalled fireworks violate the ban for aerial fireworks devices intended to produce audible effects because they have a pyrotechnic composition that exceeds the federal limit, …
Company / brand: Bada Boom Fireworks recalls
Official ID 26566 · Official notice ↗
The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.
Company / brand: 7111495 Canada recalls
Official ID 26565 · Official notice ↗
The pajama sets violate the mandatory safety standards for children's sleepwear, posing a risk of serious injury or death to children from burns.
Company / brand: Shenzhen City ShengRu Fu Shi Company recalls
Official ID 26564 · Official notice ↗
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to consume…
Company / brand: Shenzhen Fuxiangyue Technology Co recalls
Official ID 26563 · Official notice ↗
The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The strings can reach the back of children's …
Company / brand: GOPO Toys recalls
Official ID 26562 · Official notice ↗
The recalled toys violate the small parts ban because they are intended for children under three and the small pacifier poses a deadly choking hazard to young children. In addition…
Company / brand: Huizhou Huitong Crafts Co recalls
Official ID 26561 · Official notice ↗
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
Official ID Z-2413-2026 · Official record ↗
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Company / brand: AVID Medical recalls
Official ID Z-2410-2026 · Official record ↗
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Company / brand: AVID Medical recalls
Official ID Z-2409-2026 · Official record ↗
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Company / brand: AVID Medical recalls
Official ID Z-2408-2026 · Official record ↗
Inadvertent distribution of sealed pouches that had not undergone validated sterilization.
Company / brand: AVID Medical recalls
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
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
Official ID Z-2405-2026 · Official record ↗
Sterile anchors my lack sterility assurance.
Company / brand: Boston Scientific Neuromodulation recalls
Official ID Z-2404-2026 · Official record ↗
Reusable electrodes may not meet expected performance levels.
Company / brand: Boston Scientific Neuromodulation recalls
Official ID Z-2403-2026 · Official record ↗
Reusable electrodes may not meet expected performance levels.
Company / brand: Boston Scientific Neuromodulation recalls
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
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
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
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
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
Official ID Z-2362-2026 · Official record ↗
The cannulation of the CCS screw is not centered.
Company / brand: Medartis AG recalls
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
Official ID Z-2356-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.