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. 1,788 recalls have been distributed to New Jersey in the last 12 months.
Showing 41701–41720 of 53,621 recalls
Recalled Item: Orthopedic Split Drape Pack - contains Devon Light Glove Used during surgery...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye Pack - contains Devon Light Glove Used during surgery Recalled by...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abdominal Pack and Abdom Pack - contains Devon Light Glove Used during...
The Issue: Convenience kits being recalled due to the recall by the manufacturer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Perspective Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software bugs in VC20B SP0a or SP1 software versions may cause issues that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 16 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software bugs in VC20B SP0a or SP1 software versions may cause issues that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOMATOM Emotion 6 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Software bugs in VC20B SP0a or SP1 software versions may cause issues that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Systems LOCI Thyroid Stimulating Hormone Recalled by Siemens...
The Issue: Dimension Vista LOCI Thyroid Stimulating Hormone (TSH) Lot 14237AA may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IC-GREEN (indocyanine green for injection Recalled by Akorn, Inc. Due to...
The Issue: Subpotent Drug: Low out-of-specification potency result of the drug product.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tibial Alignment Guide Recalled by Zimmer CAS Due to Zimmer CAS has...
The Issue: Zimmer CAS has determined that the potential exists for the spikes on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chlordiazepoxide HCl/Clidinium Bromide capsules Recalled by Valeant...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Librax (5 mg chlordiazepoxide HCl and 2.5 mg clidinium bromide) capsules...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DeRoyal(R) Medium Specimen Retrieval Bag Recalled by DeRoyal Industries Inc...
The Issue: The firm received reports of specimen retrieval bags tearing, ripping, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL Command Modules Recalled by Spacelabs Healthcare Inc Due to...
The Issue: Ultraview SL Command Modules which were upgraded with the Masimo SpO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEBSTER HIS Catheter Recalled by Biosense Webster, Inc. Due to The Webster...
The Issue: The Webster HIS catheter, 4Pole Fixed Curve with Auto ID, is not being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: High out of specification dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Regular Strength Comfort Gel Cherry Flavor Recalled by...
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Maximum Strength Comfort Gel 12 FL OZ (355 mL) bottle...
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Regular Strength Antacid Liquid Recalled by Tarmac...
The Issue: Products failed the Antimicrobial Effectiveness Test.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hitachi Echelon MRI System Recalled by Hitachi Medical Systems America Inc...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI System Recalled by Hitachi Medical Systems America Inc Due...
The Issue: Image data transferred from the MRI system to a workstation showed errors on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.