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. 2,748 recalls have been distributed to New Jersey in the last 12 months.
Showing 17721–17740 of 53,621 recalls
Recalled Item: Medtronic Affinity Pixie Hollow Fiber Oxygenator and Cardiotomy/Venous...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Pack EVNP Clinical with AP40 1/B (PERFUSION M448036B...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable cardioverter defibrillators (ICD) with cardiac resynchronization...
The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coronavirus antigen detection test system - Product Usage: intended for...
The Issue: Two lots of test strips failed QC testing using blank buffer due to false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR...
The Issue: A small percentage of implanted cardiac devices, from a well-defined subset,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista HDLC - colorimetric method Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thread-like wire marker Recalled by Somatex Medical Technologies GMBH Due to...
The Issue: This recall has been initiated due to the risk of wire splintering after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....
The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....
The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by Teligent Pharma, Inc....
The Issue: Failed Impurities/ Degradation Specifications - OOS for know impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enoxaparin Sodium Injection Recalled by Apotex Corp. Due to Labeling; Label...
The Issue: Labeling; Label Mixup; syringe barrels may containing markings for 150 mg/mL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enoxaparin Sodium Injection Recalled by Apotex Corp. Due to Labeling; Label...
The Issue: Labeling; Label Mixup; syringe barrels may contain markings for 100 mg/mL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliVue MX40 Patient Monitor Recalled by Philips North America Llc Due to...
The Issue: Manufacturing failed to follow process steps resulting in the distribution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Custom Ophthalmic Surgical Procedure Packs Recalled by Alcon Research,...
The Issue: Reports have been received concerning mold found on gowns included in custom...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Scott¿ Moisturizing Foam Hand Sanitizer Recalled by Kimberly-Clark...
The Issue: Labeling; Label Mix-up; some bottles containing Foam Skin Cleanser soap are...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Feth-R-Kath Catheter Recalled by Epimed International, Inc. Due to Outer...
The Issue: Outer coating of the catheter may deteriorate and result in the coating to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Velocity Disposable Bipolar Ablators - Product Usage: intended to be...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed Disposable Bipolar Ablators - Product Usage: intended to be Recalled...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HNM Disposable Bipolar Ablators - Product Usage: intended to be used for...
The Issue: There can be a potential breach of the sterile packaging barrier due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Auryxia (ferric citrate) tablets Recalled by Akebia Therapeutics dba Keryx...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.