Product Recalls in New Jersey
Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,820 recalls have been distributed to New Jersey in the last 12 months.
Showing 8001–8020 of 53,621 recalls
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP Recalled by Zydus...
The Issue: Failed Dissolution Specifications-out-of-specification (OOS) test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Strong Iodine Solution U.S.P. (Lugol's Solution) (Iodine 5%) Recalled by...
The Issue: CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mini Fruit Jelly Cups Recalled by Tiffany Food Corp. Due to Products are a...
The Issue: Products are a choking hazard
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mini Fruit Jelly Cups Recalled by Tiffany Food Corp. Due to Products are a...
The Issue: Products are a choking hazard
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mini Fruit Jelly Cups Recalled by Tiffany Food Corp. Due to Products are a...
The Issue: Products are a choking hazard
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Alinity i Processing Module The Alinity i Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity c Processing Module The Alinity c Processing Recalled by Abbott...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 Processing Module 02P24-02 02P24-40 01R24-56 01R25-56...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Blood Analysis System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed a potential issue that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott CELL-DYN Ruby Recalled by Abbott Laboratories Due to The devices...
The Issue: The devices contain a dry natural rubber (latex) subcomponent, which are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Clean Stool Transportation System-For the collection...
The Issue: Due to a manufacturing defect, certain Para-Pak vials may be at risk for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Para-Pak Zn-PVA/10% Formalin-for the routine collection Recalled by Meridian...
The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Para-Pak Clean Vial-For the collection Recalled by Meridian Bioscience Inc...
The Issue: Plastic vials contain a manufacturing defect may cause an increased risk of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit - For access to the subarachnoid Recalled by...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial access kit (without Prep solutions) Bit and Guard-For...
The Issue: Defect in the outer packaging of the Cranial Access Kits can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Modular Cooler-Heater Recalled by CardioQuip, LLC Due to There is...
The Issue: There is a potential for the heating-chamber to malfunction resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioQuip Modular Cooler-Heater Recalled by CardioQuip, LLC Due to There is...
The Issue: There is a potential for the heating-chamber to malfunction resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra¿ Cranial Access Kit-For access to the subarachnoid space or Recalled...
The Issue: Defect in the outer packaging of the Cranial Access Kits. can cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.