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. 2,564 recalls have been distributed to New Jersey in the last 12 months.
Showing 43261–43280 of 53,621 recalls
Recalled Item: "***SLIM X LEAN HOUR 12+ HOUR ENERGY***PRODUCT ID: ASL-SXL-03***Manufactured...
The Issue: This product is being recalled due to the presence of undeclared synthetic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BELVIQ¿ (Lorcaserin HCl) Tablets Recalled by Eisai Inc Due to...
The Issue: Labeling:Missing Label: Bottles may not have a product label, or have a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Safeway Select French Salted Caramel (Fleur De Sel) Premium Ice Cream...
The Issue: The recipe's caramel cups ingredient was replaced with peanut butter cups...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: INRatio Monitors - 0100004 Alere INRatio PT/INR System Professional -...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G- Series Beds Recalled by Invacare Corporation Due to Invacare identified...
The Issue: Invacare identified that the rail mounting bracket on the G29 full length...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INRatio 2 Monitors - 0200431 Alere INRatio 2 PT/INR Professional Recalled by...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere INRatio PT/INR Test Strips Recalled by Alere San Diego, Inc. Due to In...
The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IS3000 Vision Side Cart (VSC) used in conjunction with the Recalled by...
The Issue: Intuitive Surgical is initiating a voluntary correction related to da Vinci...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensei X Robotic Catheter System Recalled by Hansen Medical Inc Due to The...
The Issue: The Set Up Joint subassembly of the Sensei X Robotic Catheter System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle Recalled by...
The Issue: There is the potential for a breach in the inner or outer packaging pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...
The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona Cemented Tibial Broach Inserter/Extractor. The Persona Cemented...
The Issue: The affected lot was supplied by contract manufacturer and are potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...
The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eye Drops Industrial Strength (Polyethylene glycol 400 1% Recalled by K C...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product failed a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets Recalled by Micro Labs Usa, Inc S Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Product failed a known...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops (Tetrahydrozoline HCl 0.05%) Recalled by K C Pharmaceuticals Inc...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops Advanced Relief (Dextran 70 0.1% Recalled by K C Pharmaceuticals...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Drops A.C. (Tetrahydrozoline HCl 0.05% Recalled by K C Pharmaceuticals...
The Issue: CGMP Deviations: Active Pharmaceutical Ingredient (API) used for manufacture...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.