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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 27881–27900 of 53,621 recalls
Recalled Item: Melanie Mini Cookies with Caramel Flavor in a 17.6 oz Recalled by Desly...
The Issue: Products contain undeclared peanuts.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Broccoli cuts Recalled by Ahold USA Due to Potential Listeria Contamination
The Issue: Ahold Delhaize received a report from State of CT of finding significant...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: REPLANT 5.0mmD ABUTMENT Recalled by Implant Direct Sybron Manufacturing, LLC...
The Issue: Due to out of specification, the clinician would not be able to fit and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmniSure ROM Test under the following labels: 1) Catalog Number Recalled by...
The Issue: Potential for control line not appearing on the test strip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Recalled...
The Issue: Natus Neuro has discovered a possible manufacturing defect in the ErgoJust...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNI Hip System Recalled by OMNIlife science Inc. Due to The Internal...
The Issue: The Internal packaging, the pouch and patient labels are improperly labeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS TipTracker Stylet Accessory Recalled by Arrow International Inc Due to...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VPS Rhythm ECG Accessory Pack with Johans Adapter Recalled by Arrow...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Peripherally Inserted Midline Catheter Kit with Placement Wire Recalled by...
The Issue: Product pouch label may not easily identify the lot number, expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziyad Brand Tahini Recalled by Ziyad Brothers Importing, Inc. Due to...
The Issue: Ziyad Brothers Importing is voluntarily recalling its Ziyad Brand Tahini, 8...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 7K capsules packaged in single packs sold in 24-count boxes Recalled by...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Way (Levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...
The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: My Way (levonorgestrel) Tablets TWO PACK Recalled by Lupin Pharmaceuticals...
The Issue: Marketed Without an Approved NDA/ANDA: 2-pack configuration did not receive...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: POSEIDON Xtreme PLATINUM 4500 Recalled by Shoreside Enterprises Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found products to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: screamin' menthol (menthol) Pain Relieving Gel Recalled by Ideaz Llc Due to...
The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: screamin' hot (capsaicin) Pain Relieving Gel Recalled by Ideaz Llc Due to...
The Issue: CGMP Deviations: Products manufactured with an ingredient that exceed the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Option Systems Antibacterial Foaming Hand Wash with .3% PCMX Recalled by...
The Issue: Microbial contamination of NonSterile Product; FDA analysis returned out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nature's Only Choice B17 BITTER RAW APRICOT EXTRACT AMYGDALIN Dietary...
The Issue: The Vitamin B17 containing product is considered to be a prescription drug,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: C3 is an in vitro diagnostic assay for the quantitative Recalled by Abbott...
The Issue: An update to the Reagents and Specimen Collection and Handling/Preparation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.