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. 2,820 recalls have been distributed to New Jersey in the last 12 months.
Showing 7101–7120 of 53,621 recalls
Recalled Item: I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm Recalled by In2Bones,...
The Issue: This Field Action is being conducted following the identification of a batch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 75mm Recalled by In2Bones,...
The Issue: This Field Action is being conducted following the identification of a batch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Catalog Nos. 6802413 (regular) and 6802915...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics,...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 3400 Chemistry System Recalled by Ortho-Clinical Diagnostics, Inc....
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics,...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Catalog Nos. 6802783 (regular) and...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Catalog Nos. 6802413 (regular) and 6802915...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Catalog Nos. 6802783 (regular) and...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 3400 Chemistry System Recalled by Ortho-Clinical Diagnostics, Inc....
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IdentiTi ALIF Standalone Interbody System: Part Number/Description...
The Issue: Due to reports of intraoperative graft bolt implantation breakages.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Schiff Reagent Recalled by EMD Millipore Corporation Due to This IVD is...
The Issue: This IVD is colorless. A customer complaint was received noting it appeared...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Gastrointestinal (GI) Panel RFIT-ASY-0116 (30 test kit)...
The Issue: Due to potential signals of increased false positive Norovirus results when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with:...
The Issue: Due to a trend in false positive Candida tropicalis results on blood culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Banana Pepper Rings 16 FL OZ (1PT) 473ml . Packaged Recalled by Lidl US...
The Issue: Container integrity issued (punctured lid)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Authentic Fresh to You Deluxe Triple Decker Club Net Wt. Recalled by MG...
The Issue: Undeclared egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nortrel (norethindrone and ethinyl estradiol tablets USP) 0.5/35 Recalled by...
The Issue: Discoloration: discolored tablets (shades of blue) mixed in with the white...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nortrel 7/7/7 (norethindrone and ethinyl estradiol tablets USP- triphasic...
The Issue: Discoloration: discolored tablets (shades of blue) mixed in with the white...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.