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. 2,789 recalls have been distributed to North Carolina in the last 12 months.
Showing 7301–7320 of 54,363 recalls
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...
The Issue: New warnings are being added to the Instructions for Use for all affected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...
The Issue: IFU has been updated to include warnings about the risk of the inlet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Divalproex Sodium Extended-release Tablets Recalled by Amneal...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg Recalled by...
The Issue: Microbial Contamination of Non-Sterile Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benzonatate Capsules Recalled by Amerisource Health Services LLC Due to...
The Issue: Superpotent drug: Assay results were slightly above specification at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Senographe Pristina Recalled by GE Medical Systems, SCS Due to X-ray...
The Issue: X-ray exposure termination audible signal on Senographe Pristina with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...
The Issue: Knee batteries may need replacement with conforming batteries to ensure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling
The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling
The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Exactamix Pro 1200 Recalled by Baxter Healthcare Corporation Due to...
The Issue: An error was identified in software versions 2.0.8 and 2.1.8 while using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Exactamix Pro 2400 Recalled by Baxter Healthcare Corporation Due to...
The Issue: An error was identified in software versions 2.0.8 and 2.1.8 while using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use Recalled by...
The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use...
The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Popcorn Pre-Pop in 8oz Polypropylene bag packaged 20 bags to a case Recalled...
The Issue: Undeclared Yellow #5
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Americaine Recalled by Insight Pharmaceuticals LLC, a Prestige Consumer...
The Issue: Chemical Contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.