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. 1,117 recalls have been distributed to North Carolina in the last 12 months.
Showing 7521–7540 of 54,363 recalls
Recalled Item: bkActiv Ultrasound System 2300 Recalled by B-K Medical A/S Due to An issue...
The Issue: An issue on the Dual Live Compare feature on the bkActiv system could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE Recalled by...
The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 9251R1 Recalled by Busse Hospital Disposables, Inc. Due to Firm...
The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GammaPod - Treatment Planning System-a component of the GammaPod Irradiation...
The Issue: Wrong structures imported into the GammaPod Treatment Planning...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE Recalled by...
The Issue: Firm is recalling all kits containing recalled lots of Nurse Assist Sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView Recalled by Philips North America Due to While using...
The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT Recalled by Philips North America Due to While using...
The Issue: While using Pre-Programmed Motion during an extrinsic quality assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedural convenience kits and trays Recalled by American Contract Systems,...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RX Series Copper (Cu) Assay Ref. Number CU2340 Recalled by Randox...
The Issue: Randox Laboratories have released an update to the Carryover Avoidance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.