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. 1,777 recalls have been distributed to New Jersey in the last 12 months.
Showing 46301–46320 of 53,621 recalls
Recalled Item: Zoll Medical X Series Recalled by ZOLL Medical Corporation Due to...
The Issue: Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEVION S250 Recalled by Mevion Medical Systems, Inc. Due to Geometric...
The Issue: Geometric positioning error can occur after a rotational correction has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....
The Issue: Extremely low absorbance readings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Symbia T and Symbia T2 computer tomography systems. These systems Recalled...
The Issue: There are confirmed reports of a component coming loose inside the CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....
The Issue: Extremely low absorbance readings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Oxylog 3000 plus ventilators Recalled by Draeger Medical Systems,...
The Issue: The potentiometers (knobs) for setting the ventilation parameters may have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl 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: THC 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: Adeno/Rota Combo 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: MDMA/Ecstasy 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: MDMA/Ecstasy 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: Strep A 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: Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800...
The Issue: Sterility of the product cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Malaria pan Antigen Test 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: Fentanyl 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: Morphine Strips (2000) 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: Adenovirus 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: Benzodiazepine 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: Fecal Occult Blood 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: Cocaine 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.