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. 2,551 recalls have been distributed to New Jersey in the last 12 months.
Showing 46381–46400 of 53,621 recalls
Recalled Item: Fecal Occult Blood 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: Barbiturate Test Card 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: Buprenorphine 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: Oxycodone Test Card 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: Dengue NS1 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: Salmonella typhi/paratyphi Antigen Test Recalled by LumiQuick Diagnostics...
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: Rickettsia IgG/IgM Test Card LumiQuick Recalled by LumiQuick Diagnostics...
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: Cardiac Panel Test Card (Whole Blood) Recalled by LumiQuick Diagnostics Inc....
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: EDDP Strip Recalled by LumiQuick Diagnostics Inc. Due to Products shipped 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: H. Pylori Antigen Test Card LumiQuick Recalled by LumiQuick Diagnostics Inc....
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: PCP Test (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: Methadone Test 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: HeartMate II System Controller Product Usage: HeartMate II is a Recalled by...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II LVAD Pump and Pock Controller Kit Recalled by Thoratec...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heart Mate II Pocket Controllers removed from packaging Product Usage:...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II Implant Kit with Pocket Controller Recalled by Thoratec...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your 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.
Recalled Item: Pleo Quent DROPS 5X 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.