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. 1,932 recalls have been distributed to North Carolina in the last 12 months.
Showing 20541–20560 of 29,737 recalls
Recalled Item: Brilliance 16 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance BigBore Radiology CT Model number 728244 Product Usage: Computed...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 16 Power Recalled by Philips Medical Systems (Cleveland) Inc...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Recalled by...
The Issue: Incorrect drill protocol in the Instructions for Use (IFU)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BLUE IMPERVIOUS GOWN WITH THUMBHOOKS Recalled by Cardinal Health Due to Blue...
The Issue: Blue Impervious Gown with thumbhooks, X-large. All lots do not meet design...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 CT Model number 728231 Product Usage: Computed Tomography...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva with Flat Detector Recalled by Philips Electronics North...
The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva Recalled by Philips Electronics North America...
The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGR Matrix Surgical Mesh Recalled by Novus Scientific Ab Due to Novus...
The Issue: Novus Scientific is implementing additions to the product's instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: Recalled by...
The Issue: Sterility compromised due to breach in sterile packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroDiagnost Recalled by Philips Electronics North America Corporation Due to...
The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fusion ENT Application. The software application is sent in CD Recalled by...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NOMAD Pro2 Packaged X-Ray System Recalled by Aribex Inc Due to Firm received...
The Issue: Firm received customer complaints where end users reported that Nomad Pro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-450NR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVX-450BR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MACH Cranial Treon. The software application is sent in CD format with an...
The Issue: Medtronic Navigation, Inc. announces a voluntary field action for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD) Recalled by Becton, Dickinson...
The Issue: Internal review found that some vials of CD3/CD4/CD45 state that the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.