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. 1,824 recalls have been distributed to North Carolina in the last 12 months.
Showing 38741–38760 of 54,363 recalls
Recalled Item: Dressol-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...
The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressit-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...
The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA...
The Issue: PMMA is listed as a material on the label but the product does not contain PMMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Fuhrman Pleural/Pneumopericardial Drainage Set The Fuhrman...
The Issue: Stryker Sustainability Solutions is recalling the Fuhrman Pleural &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Imaging XS is a Picture Archiving and Communication System (PACS)...
The Issue: For the Syngo Workflow SLR System with Software Ver: VB10C: Printouts may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Recalled by...
The Issue: Some tubes were manufactured with the stopper not fully inserted into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II...
The Issue: A damaged temperature sensor at the ENDOEYE tip caused the distal end to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaPACS Diagnostic Viewer versions 8.3.7 Recalled by Novarad Corporation...
The Issue: The SUV values that are being calculated in the PET/CT fusion tool are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIRMINGHAM HIP RESURFACING MODULAR HEAD Recalled by Smith & Nephew, Inc. Due...
The Issue: The 16 devices distributed in the United States were incorrectly labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugSmart Cup 10 Recalled by Ameditech Inc Due to Ameditechs Drugs of Abuse...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11 Panel Card (OPI 300) w/Adult Recalled by Ameditech Inc Due to Ameditechs...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImmuTest Cup 7-panel w/ Adulteration Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen CLIA Waived Cup with 6 Drugs Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immutest 12 Panel Cup w/Adulteration Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immutest 10 Pnl Drug Screen Cup w/ Adult Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.