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. 1,120 recalls have been distributed to New Jersey in the last 12 months.
Showing 12501–12520 of 53,621 recalls
Recalled Item: Freeman Pancreatic Flexi-Stent (contained in kit 6501) Catalog Number: 6541...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6567 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Helical Retrieval Basket Catalog Number: 4808 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6001...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6562 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Helical Retrieval Basket Catalog Number: 4816 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4704 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits Catalog Number: 6104 Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6567) Catalog Number: 6519...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4563-OLY Recalled by Hobbs...
The Issue: Device label display an incorrect expiration date, extends the shelf life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Banana Boat hair & scalp defense Recalled by Edgewell Personal Care Brands,...
The Issue: Chemical contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin Capsules Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations:OOS result was observed in 1-Methyl-4-Nitroso Piperazine...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Divalproex Sodium Extended Release Tablets Recalled by Amneal...
The Issue: Failed dissolution specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azacitidine for Injection Recalled by Amerisource Health Services LLC Due to...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Barco Medical Network Adapter Recalled by BARCO NV Due to installation issues
The Issue: installation issues
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SWANSON Flexspan Finger Joint Implant W/O Grommets Silicone Recalled...
The Issue: An incorrect sizing label was applied to the carton packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T and 2008TBluestar Hemodialysis Machines with CDX-Indicated for acute...
The Issue: (1)Software version 2.74 upgrade and (2)hardware related cause that affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORCA FOAM STANDARD CUBE 10x10x10 mm Recalled by GELITA MEDICAL GMBH Due to...
The Issue: In routine bioburden testing, higher than acceptable levels of Endotoxins...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.