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. 2,557 recalls have been distributed to New Jersey in the last 12 months.
Showing 44461–44480 of 53,621 recalls
Recalled Item: Transport Rollator with Padded Seat Recalled by Roscoe Medical Inc Due to...
The Issue: The caster may separate completely from the device frame causing injury to user.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Puritan Bennett 980 Ventilator Recalled by Nellcor Puritan Bennett...
The Issue: Covidien is recalling certain Puritan Bennett 980 Ventilator Systems due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuum Acetabular System Trabecular Metal Shell with Multi Holes Recalled...
The Issue: The affected products are missing polar boss threads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...
The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spline Twist Implant Recalled by Zimmer Dental Inc Due to Zimmer Dental is...
The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee...
The Issue: Packaging of a device was compromised
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension HB1C Flex reagent cartridge Recalled by Siemens Healthcare...
The Issue: Certain lots of the reagent cartridges show confirmed positive bias...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Masimo SET uSpO2 Cable The Masimo SET uSpO2 Pulse Oximetry Recalled by...
The Issue: Firm has identified a small number of Oximetry Cables with crossed-internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Truvada (200 mg emtricitabine and 300 mg tenofovir disoproxil fumarate)...
The Issue: Presence of Foreign Substance: Truvada was found to contain small red...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Elk shaped pasta Ekologiska PASTA-ALGAR FULLKORN Pasta elks wholemeal...
The Issue: Pasta-Algar and Pasta-Algar Fullkorn are recalled due to undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Elk shaped pasta Ekologiska PASTA-ALGAR Pasta elks Recalled by Ikea North...
The Issue: Pasta-Algar and Pasta-Algar Fullkorn are recalled due to undeclared soy.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DOPamine Hydrochloride and 5% Dextrose INJ Recalled by Baxter Healthcare...
The Issue: Lack of Assurance of Sterility: A small cut in the solution bag may have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CADD-Solis Medication Safety Software Recalled by Smiths Medical ASD, Inc....
The Issue: Smiths Medical has identified an issue with a single batch (Lot Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Selector Kit Sterile single use device A bi-lumen Recalled by...
The Issue: Some specific lots of Selector Tubing may potentially leak irrigation fluid...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Software Version 3.1 utilized on the following systems: 1) Recalled...
The Issue: Calibration may not occur when using calibrator barcode labels supplied with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coloplast Conveen Urine Collection Leg Bag Recalled by Coloplast...
The Issue: Coloplast is recalling the Conveen Contour Leg Bag due to potential leakage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Healthcare Recalled by Merge Healthcare, Inc. Due to It has been...
The Issue: It has been reported that during use, the SpO2 value displayed on the Hemo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Saturated Gauze Dressing Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Black Mamba Suture Passer. The Biomet Sports Medicine Mamba instruments...
The Issue: An investigation identified that high level friction may exist between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amerigel Daily Dressing Packets Wound management Recalled by Amerx Health...
The Issue: Formulation deviation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.