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. 2,683 recalls have been distributed to New Jersey in the last 12 months.
Showing 20981–21000 of 29,496 recalls
Recalled Item: POROUS PATELLA 32MM X 10MM - 00587806532 POROUS PATELLA 35MM Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM Image Suite V4 Recalled by Carestream Health Inc Due to...
The Issue: Carestream Health received a complaint related to CARESTREAM Image Suite 4...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liver Access and Biopsy Needle Set Biopsy needle kit Intended Recalled by...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TM CR TIB SZ 3 C-H Recalled by Zimmer Trabecular Metal Technology, Inc. Due...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Therapy Foot Wrap Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volt Resistance Heated Lower Back Garment Deep penetrating heat garment...
The Issue: During an FDA inspection it was found that the firm claims unapproved...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Selective Salpingography Catheter with Beacon Tip Cannula Recalled by Cook...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Slip-Cath Beacon Tip Catheter Catheter Recalled by Cook Inc. Due to Increase...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transluminal Biliary Biopsy Forceps Set Forceps Recalled by Cook Inc. Due to...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REV. SHELL LINER 0D 28X48 00700504828 REV. SHELL LINER 10D Recalled by...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Given Imaging Bravo¿¿ pH capsule delivery device Recalled by Covidien LLC...
The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: White Lumax Guiding Coaxial Catheter Catheter Recalled by Cook Inc. Due to...
The Issue: Increase in reports of polymer degradation of the catheter tip, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Given Imaging Bravo¿ pH capsule delivery device Recalled by Covidien LLC Due...
The Issue: Potential of an allergic reaction in a patient with nickel sensitivity.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge LIS software. The firm name on the label is Recalled by Merge...
The Issue: There are potential issues with results reporting for certain run-based...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to Potential...
The Issue: Potential non-recoverable loss of image acquisition. The affected Discovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00720504022 ACETAB.CUPW/SH Recalled by Zimmer Trabecular Metal Technology,...
The Issue: Zimmer Biomet is initiating a recall of specific lots of foil pouched,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated...
The Issue: Due to a packaging error; The kit does not contain the correct number of C1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision R Recalled by Ziehm Imaging Inc Due to Malfunction of the...
The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ziehm Vision RFD 3D Mobile C-arm for Mobile Fluoroscopic Imaging Recalled by...
The Issue: Malfunction of the radiation-warning timer and the 3D-specific interval...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.