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. 2,632 recalls have been distributed to New Jersey in the last 12 months.
Showing 34261–34280 of 53,621 recalls
Recalled Item: McConnell's Fine Ice Cream Salted Caramel Chip Recalled by McConnell's Ice...
The Issue: Potential Listeria monocytogenes contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BON APPETITO WALNUT LADIES FINGER Recalled by Golden Star International Inc....
The Issue: Undeclared Eggs and Soy Oil/Lecithin
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Synthes 0.76 mm Drill Bit/Stryker J-Latch/with 5mm Stop/44.5 mm Non-Sterile...
The Issue: Package may be incorrectly labeled as containing 0.76 mm Drill Bit, but in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/zeego Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility exists that the semi-automatic focus switch may not work as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC unit Recalled by CareFusion 303, Inc. Due to Reports where...
The Issue: Reports where the Low Battery alarm and/or the Very Low Battery alarm are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol 80 Mcg Recalled by Teva...
The Issue: Failed Content Uniformity: Product was out of specification for spray...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility: Complaints of broken tips on the ampules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol 40 Mcg Recalled by Teva...
The Issue: Failed Content Uniformity: Product was out of specification for spray...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MEVION S250 Product Usage: Proton Radiation Therapy Recalled by Mevion...
The Issue: Completing Setup Without Program Move Complete Can Cause An Isocenter Error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MSS CASSETTE GLU/LAC/UREA (BUN) as a part of the Roche Recalled by Roche...
The Issue: Incorrect Urea results may be generated sporadically on cobas b 221<6>Roche...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Turbo Elite Atherectomy Catheter. Models: 410-152 Recalled by Spectranetics...
The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medi Choice Arm Slings ASL 2103 Small 7.5 x 12.5 Inch 1/EA Recalled by Owens...
The Issue: Owens & Minor is the initial importer and private label distributor of Medi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELCA Coronary Atherectomy Catheter. Models: 110-001 Recalled by...
The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bridge Occlusion Balloon. Model: 590-001 Temporary vessel occlusion of the...
The Issue: Spectranetics Corporation announces a voluntary field action for the Turbo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Flexible Shaft Recalled by Synthes (USA) Products LLC Due to...
The Issue: Non-conforming material used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perceval Sutureless Aortic Heart Valve size S Recalled by Sorin Group USA,...
The Issue: Sorin Group USA, Inc. announces a voluntary field action for the Perceval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SURESOUND22US Multipack (US Distribution) containing 2 packs of six devices....
The Issue: Breach in sterile barrier compromising product sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S...
The Issue: A change in the calibration curve causing an increase in false prozone flags.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.