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. 1,139 recalls have been distributed to New Jersey in the last 12 months.
Showing 10401–10420 of 29,496 recalls
Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...
The Issue: Customers were not notified of previous recalls associated with various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In2Bones Shannon Percutaneous Burr - Product Usage: indicated for forefoot...
The Issue: This Field Action is being conducted following identification of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magellan 3 mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...
The Issue: Safety shield not locking into the cannula. If the safety shield activation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...
The Issue: Customers were not notified of previous recalls associated with various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to Customers were not...
The Issue: Customers were not notified of previous recalls associated with various...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mizuho CE IPX4 Recalled by Mizuho OSI Due to There is a potential that hand...
The Issue: There is a potential that hand control units may cause the tabletop to slide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ImmunoCard Mycoplasma EIA detects the presence of IgM to Recalled by...
The Issue: Use of the kits after incorrect storage could lead to a potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enzyme linked immunosorbent assay Recalled by Siemens Healthcare...
The Issue: Potential false positive HSV results. Siemens Healthcare Diagnostics, Inc....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 870 DR Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 850 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NM/CT 860 Nuclear Medicine / CT Scanners Recalled by GE Healthcare, LLC Due...
The Issue: GE Healthcare has become aware of a potential issue on 800 family NM/CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methamphetamine Intercept Microplate kit EIA - IVD qualitative determination...
The Issue: Incorrect lot of Substrate Reagent (TMB) may be included in the kit. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000C Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000F Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System INFX-8000V Recalled by Canon Medical System, USA, INC. Due to The...
The Issue: The x-ray irradiation field may shift with respect to image receiving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Pack EVNP Clinical with AP40 1/B (PERFUSION M448036B...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Affinity Pixie BP241 Hollow Fiber Oxygenator and Cardiotomy/Venous...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Perfusion System (CUSTOM PACK BB10H89R4 ECLR). The Affinity Pixie...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Affinity Pixie Hollow Fiber Oxygenator and Cardiotomy/Venous...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Pack CP Kinderset 1/4-1/4 MIT Pixie 1/B (PERFUSION Recalled...
The Issue: Products being recalled due to potentially elevated level of bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.