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. 2,786 recalls have been distributed to New Jersey in the last 12 months.
Showing 13341–13360 of 29,496 recalls
Recalled Item: BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 Recalled by...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs Recalled...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Groshong 9.5 Dual-Lumen CV Catheter Recalled by Bard Peripheral Vascular...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accutorr 3 Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rosebud Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rosie4 Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accutorr 7 Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System - Product Usage: Indicated for...
The Issue: Power supply (Model Number: TLC-2003) ME90A2403F01 (24 VDC, 3.75 A, 90 W, 1%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...
The Issue: Device was shipped without a Unique Device Identification (UDI) label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLC-2000 Therapeutic Medical Laser System Recalled by Theralase Inc. Due to...
The Issue: Device was shipped without a Unique Device Identification (UDI) label and a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torrent Suite Dx Software Version 5.8 Catalog Number:A36601 and A36602...
The Issue: Torrent SuiteTM Dx analysis software, a component of the Ion PGM Dx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.