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. 2,789 recalls have been distributed to North Carolina in the last 12 months.
Showing 7661–7680 of 29,737 recalls
Recalled Item: Cardinal Health GEL PACK REUSABLE Recalled by Cardinal Health 200, LLC Due...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health HOT AND COLD GEL PACK REUSABLE Recalled by Cardinal Health...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health INSULATED GEL PACK REUSABLE Recalled by Cardinal Health 200,...
The Issue: Users are being informed that the product should not be used on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zio AT Clinical Manual Recalled by iRhythm Technologies, Inc. Due to...
The Issue: Ambulatory ECG monitoring system labeling update: 1) Clinically actionable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEED 9X10X10mm Continuous Compression Implant Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Synthes Hammertoe Continuous Compression Implants Recalled by Synthes...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEEDSHIFT20x20x20 Offset 10mm Implant Drill Kit Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPEED 15X12X12mm Continuous Compression Implant Recalled by Synthes (USA)...
The Issue: The subject products are being recalled because they contain the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Recalled by...
The Issue: GAGA Pro LLS systems was not in compliance with the FDA's Performance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LumiraDx SARS-CoV-2 Antigen (Ag) Liquid Quality Control Kit Catalog #:...
The Issue: Assigned vial lot numbers for the incorrect type of product. SARS-CoV-2 &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-C6 Recalled by Hamilton Medical AG Due to Due to a malfunction...
The Issue: Due to a malfunction related to the backlight on the ventilator screen. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoPulse Li-ion Battery used on the AutoPulse Resuscitation System Model...
The Issue: Due to increase in Li-Ion Battery failures
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WEB Detachment Controller Recalled by MICROVENTION INC. Due to Detachment...
The Issue: Detachment controller, of an aneurysm embolization system, has an out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GORE CARDIOFORM ASD Occluder. cardiovascular implant. Recalled by W L Gore &...
The Issue: Due to manufacturing records (Release Test Results) indicating "Failed".
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711 Recalled...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex Medical RUSCH Pocket Pac i.c. Closed System Intermittent Catheter...
The Issue: Product may not be sterile
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Pump/Model: MiniMed 630G/ MMT-1715 Recalled by Medtronic MiniMed Due...
The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci X (IS4200) and Xi (IS4000) systems Recalled by Intuitive Surgical,...
The Issue: Inadvertent energy delivery from surgical system instrument if 1) Force...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vortex MP Port Titanium Low Profile Implanted Port with 5F Recalled by...
The Issue: Printed Instructions for Use (IFU) not shipped with device. The Instructions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has become aware of three potential software issues with ARTIS pheno...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.