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. 2,653 recalls have been distributed to New Jersey in the last 12 months.
Showing 25641–25660 of 29,496 recalls
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: FAS-LOC 6 Foot Disposable Extension Cable with Safe Connect/Screw Down....
The Issue: Remington Medical discovered an error on the FL-601-97 IFU; part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DPM 6 Monitor in use with a Multi Parameter Module Recalled by Mindray DS...
The Issue: The MPM included a cardiac ST/Arrhythmia analysis feature which is not...
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: 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: Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant....
The Issue: The outer package label contained the incorrect length of the device. There...
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: Rotavirus Test Card LumiQuick 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: PCP Test Card 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: 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: 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: 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 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: 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: 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: Morphine Test Card (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: 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: 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: 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.