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. 1,822 recalls have been distributed to North Carolina in the last 12 months.
Showing 41041–41060 of 54,363 recalls
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 200 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 365 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 150 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stripper Recalled by American Medical Systems Innovation Center - Silicon...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts Recalled by Synthes,...
The Issue: It was reported that the RIA Drive Shaft, Tube Assembly, and Reamer Head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pull Reduction Device For 4.3mm Percutaneous Drill Guide Recalled by...
The Issue: Certain affected parts and lots of the Pull Reduction Devices may have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z-CAT Dry Barium Sulfate for Suspension (2% w/w after mixing) Recalled by...
The Issue: Failed stability specifications:This recall has been initiated due to out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glucosamine 750 mg 120 ct Recalled by Novacare, LLC Due to TSN Labs is...
The Issue: TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PTW UNIDOS webline: 1) Recalled by PTW-Freiburg Due to In some cases,...
The Issue: In some cases, especially with high dose-per-pulse-rates typical for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation 4.7 Recalled by RAYSEARCH LABORATORIES AB Due to Issue with the...
The Issue: Issue with the algorithm for ROI contraction in RayStation 4.7 when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cortical Pin 2.0 mm Recalled by Musculoskeletal Transplant Foundation, Inc....
The Issue: Musculoskeletal Transplant Foundation (MTF) is recalling one lot of MTF's...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.