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. 970 recalls have been distributed to New Jersey in the last 12 months.
Showing 46381–46400 of 53,621 recalls
Recalled Item: Barbiturate Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malaria pf Antigen Test Card Recalled by LumiQuick Diagnostics Inc. Due to...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cocaine Strip Recalled by LumiQuick Diagnostics Inc. Due to Products shipped...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tramadol Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Myoglobin Test Card (Serum) Recalled by LumiQuick Diagnostics Inc. Due to...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Buprenorphine Test Strip Recalled by LumiQuick Diagnostics Inc. Due to...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dengue IgG/IgM Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H. Pylori Ab Test Card-Serum Recalled by LumiQuick Diagnostics Inc. Due to...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drugs of Abuse Panel Test Device Recalled by LumiQuick Diagnostics Inc. Due...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Propoxyphene Test Strip Recalled by LumiQuick Diagnostics Inc. Due to...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketamine Strip Recalled by LumiQuick Diagnostics Inc. Due to Products...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcohol Test Recalled by LumiQuick Diagnostics Inc. Due to Products shipped...
The Issue: Products shipped to US locations that do not have approved applications for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoledronic Acid Injection 5 mg per 100 mL (0.05 mg/mL) Recalled by Sagent...
The Issue: Lack of Assurance of Sterility; leaking of premix bags
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VIVITROL (naltrexone for extended-release injectable suspension) Recalled by...
The Issue: Customer complaints for failure to deliver the dose.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ritalin HCl (methylphenidate HCl) USP Recalled by Novartis Pharmaceuticals...
The Issue: Labeling: Incorrect or Missing Package Insert; The back of the Medication...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Quent CAPSULES 4X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Not PORTABLE SIPS Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.