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. 1,110 recalls have been distributed to New Jersey in the last 12 months.
Showing 14081–14100 of 53,621 recalls
Recalled Item: TETRACAINE 1% Tetracaine HCI Injection Recalled by Vitae Enim Vitae...
The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cub 2 Enclosed Bed Canopy System Recalled by Sensory Medical Inc Due to Due...
The Issue: Due potential misuse of the product, firm is updating warnings and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology Recalled...
The Issue: Atlas Stim Headbox (ASHB) was delivered to US customers under a premise that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Les Fermes Cavendish Farms Frozen Original Hash Brown Potato Patties Net Wt...
The Issue: Undeclared barley and wheat flour
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 20/30 INDEFLATOR - WPL2122268-01 (2019-03-01) Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VELYS Robotic-Assisted Solution Base Product No.: 451570100 Recalled by...
The Issue: System software v1.5.1 has a system software issue related to the Daylight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plus 30 Priority Pack w/.096 RHV - WPL2122277-01 Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 Priority Pack w/COPILOT - WPL2122272-01 (2019-03-01) Recalled by...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20/30 Priority Pack Accessory Kit/.096 RHV - WPL2122270-01 Recalled by...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INDEFLATOR Plus 30 - WPL2122277-01 (2019-03-01) Recalled by Abbott Vascular...
The Issue: Due to an increase in complaint trend for leaks and intermittent/loose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virus Counter Platform with Model Name VC3100 Recalled by Sartorius...
The Issue: The Virus Counter is an automated laboratory instrument that enables rapid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sucralfate Oral Suspension Recalled by DASH Pharmaceuticals LLC Due to...
The Issue: Labeling: Label Mix-Up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Risedronate Sodium Tablets Recalled by Macleods Pharma Usa Inc Due to FAILED...
The Issue: FAILED CONTENT UNIFORMITY SPECIFICATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gallant VR Implantable Cardioverter Defibrillator REF # CDVRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant HF Implantable Cardioverter Defibrillator REF# CDHFA500Q Recalled by...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q Recalled...
The Issue: Bluetooth malfunction impacting Gallant devices post-implant. The failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin 2 PCS MER3700 programmer Model MER3400 software Recalled by St. Jude...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...
The Issue: Due to a programmer software anomaly under very specific circumstance when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Item # 743-0278 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Item # 744-4875 Recalled by Continental Mills (Corporate Office) Due to...
The Issue: foreign materials
Recommended Action: Do not consume. Return to store for a refund or discard.