Product Recalls in North Carolina
Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,828 recalls have been distributed to North Carolina in the last 12 months.
Showing 2421–2440 of 29,737 recalls
Recalled Item: CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model...
The Issue: Potential for certain SKUs and lot numbers were distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) MTO Recalled by MEDLINE...
The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Fluid Delivery Set with Drip Chamber: 1) FDS Recalled by MEDLINE...
The Issue: Fluid Delivery Sets were incorrectly assembled with a white macro drip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LithoCrushV Single Use Mechanical Lithotriptor V. Model Number:...
The Issue: Potential for distal tip tearing of the Mechanical Lithotriptor V.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1)...
The Issue: Complaints have been received regarding post-operative implant collapse.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Premium Dressing Change Kit with Recalled...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: IMed Products Product Name: Dressing Change Kit with Recalled by...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Cloth Recalled...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Transparent...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Tacy Medical Recalled by Trinity Sterile, Inc. Due to Potential...
The Issue: Potential for hole in package compromising sterility of the medical kit.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion GBS Assay Kit containing Panther Fusion Recalled by Hologic,...
The Issue: Potential weak pouch seal on Panther Fusion GBS assay cartridge, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenTiva Recalled by LivaNova USA, Inc. Due to Vagus nerve stimulator...
The Issue: Vagus nerve stimulator generators may stop delivering stimulation due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SenTiva Recalled by LivaNova USA, Inc. Due to Vagus nerve stimulator...
The Issue: Vagus nerve stimulator generators may stop delivering stimulation due to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pediatric One-Piece Arterial Cannulae Recalled by Medtronic Perfusion...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due to...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Select Series Angled Tip Arterial Cannula Recalled by Medtronic Perfusion...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP Flex with SmartAssist Recalled by Abiomed, Inc. Due to Optical...
The Issue: Optical Sensors have been damaged due to physical interaction between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VALITUDE CRT-P Recalled by Boston Scientific Corporation Due to A subset of...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.