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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 26941–26960 of 29,496 recalls
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM/CT 670 dual detector free-geometry integrated nuclear imaging...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optima NM/CT 640 Product Usage: The GE Optima NM/CT 640 Recalled by GE...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brivo NM615 Recalled by GE Healthcare, LLC Due to GE became aware of an...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery NM 630 Recalled by GE Healthcare, LLC Due to GE became aware of an...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Infinia Hawkeye 4 Option For Dual-Head Variable Angle Gamma...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Varicam/VG and VG Hawkeye devices Product Usage: The Recalled...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Affirm VPIII Microbial Identification Tests Recalled by Becton Dickinson...
The Issue: In vitro diagnostic test kit may exhibit invalid internal negative control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elscint APEX Helix Recalled by GE Healthcare, LLC Due to GE became aware of...
The Issue: GE became aware of an incident at a VA Medical Center facility in the US in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnicycle Elite Recalled by Accelerated Care Plus Corporation Due to An...
The Issue: An anomaly in the firmware that may cause Omnicycle Elite to operate at a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes CMF Distraction System The product is intended for use Recalled by...
The Issue: The firm initiated a voluntary recall of the BC Distractor Body which is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The LIFEPAK 500 Automated External Defibrillator is a semi-automatic...
The Issue: The LIFEPAK 500 Automated External Defibrillator (AED) could be susceptible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products CRBM Slides packaged as 90 slides/pack catalog...
The Issue: Ortho Clinical Diagnostics is recalling Slide Dispense cartridges used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.