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. 1,154 recalls have been distributed to North Carolina in the last 12 months.
Showing 1001–1020 of 29,737 recalls
Recalled Item: ICU Medical ChemoLock Port w/Spiros Recalled by ICU Medical, Inc. Due to...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICU Medical ChemoLock Closed Vial Spike w/Skirt Recalled by ICU Medical,...
The Issue: Port weld of drug transfer device may separate or break during use and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Rex UNO Microinterventional Goniotomy Instrument. Model Number: CRX-120....
The Issue: Potential for compromised integrity of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyclopen Microinterventional Cyclodialysis System. Model Number: CP-300....
The Issue: Potential for compromised integrity of the sterile packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...
The Issue: Due to display cables used for monitors were not in compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flow Re-Direction Endoluminal Devices: FRED 27 Recalled by MICROVENTION INC....
The Issue: Flow diverter may have a manufacturing issue related to the tantalum length...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AW Server 2.0 Recalled by GE Medical Systems, SCS Due to Firm has identified...
The Issue: Firm has identified a security vulnerability in AW Server products. If...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...
The Issue: Due to display cables used for monitors were not in compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Branding is not applied to this product. Product Recalled by...
The Issue: Due to display cables used for monitors were not in compliance with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description FHCP08Y C SECTION PK...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description EVLH67F LEFT HEART CATH...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XERF EFFECTOR 60. Electrosurgical unit. Recalled by Lutronic Corporation Due...
The Issue: Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits IHDC30R D AND C PACK Recalled by American Contract...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon Recalled by...
The Issue: Carotid stent and post-dilation balloon system with integrated embolic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description HSLM53AB SPINE PACK MILM82A...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Basic Biopsy Tray Recalled by American Contract Systems Inc. Due to...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description BUCY78E CYSTO PACK CMCP10X...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medical convenience kits Item Number/Description RCGY52D GYN LAPAROSCOPY SPH...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Basic Biopsy Tray Recalled by American Contract Systems Inc. Due to...
The Issue: Identified products were re-gassed (sterilized more than once) after a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.