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. 2,658 recalls have been distributed to New Jersey in the last 12 months.
Showing 23901–23920 of 29,496 recalls
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Medtronic Recalled by Medtronic Neuromodulation Due to Current labeling...
The Issue: Current labeling indicates that cycling improves device longevity in every...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...
The Issue: The labelled expiration dating of the affected product is not fully...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 8100 Recalled by Carestream Health, Inc. Due to Units device head...
The Issue: Units device head descended unexpectedly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 8100 3D Recalled by Carestream Health, Inc. Due to Units device head...
The Issue: Units device head descended unexpectedly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This correction applies to all GE Healthcare MRI systems with Recalled by GE...
The Issue: At certain sites, the MRU may not be connected to the magnet. In emergency...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 6 Aseptic Housing. The Stryker System 6 Aseptic Housings Recalled by...
The Issue: Stryker is recalling System 6 Aseptic Housing, due to a failed Continuous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cold Therapy Pad - cold water circulating pad Recalled by Cincinnati...
The Issue: Seals in the water path of the CT-99 cold therapy pad may separate during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW Epidural Needle Component (product number AN-05501). Epidural needles...
The Issue: The product labeling does not specify the 5 year shelf life of the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Ebb Complete Tamponade System Recalled by Clinical Innovations, LLC Due...
The Issue: Clinical Innovations, LLC is voluntarily recalling the Ebb Complete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit. The...
The Issue: Foreign material found within the kits. The foreign material, white or black...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPWorks software used in the Xltek Protektor Stimulator Product Usage:...
The Issue: Software error occurs when using remote monitoring; if the remote user tries...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.