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 39281–39300 of 54,363 recalls
Recalled Item: Welch Allyn KleenSpec Corded Illumination System Recalled by Welch Allyn Inc...
The Issue: The firm became aware that the KleenSpec¿ 788 Corded Illuminator has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Infusion Pump (model 300000) and Triton fp Infusion Pump Recalled by...
The Issue: The device might fail to detect air in line while infusing the medication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The "Pacifier Activated Lullaby" (PAL) System composed of three major...
The Issue: PAL unit has undergone significant technological changes since the previous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kontos Falafel Mix Net Wt. 5 LBS. (2.27kg) Distributed by Kontos Foods Inc....
The Issue: Kontos Falafel Mix contains undeclared wheat allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Merge Cardio software. Merge Cardio is a system intended to Recalled by...
The Issue: Reporting feature times out after inactivity for more than an hour sending...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips X-Ray Systems Recalled by Philips Electronics North America...
The Issue: Upon initiating Fluoroscopy the user may encounter a user message Fluoro...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rhino 7 3000 Recalled by MSNV, Inc dba National Video Supply Due to...
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Tablets Recalled by Tribute Pharmaceuticals US Inc. Due to...
The Issue: Chemical Contamination: The product may contain trace amounts of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 Platinum 3000 Recalled by MSNV, Inc dba National Video Supply Due to...
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibric Acid Tablets 105 mg Recalled by Tribute Pharmaceuticals US Inc....
The Issue: Chemical Contamination: The product may contain trace amounts of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 3000 Recalled by Premiere Sales Group Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rhino 7 Platinum 3000 Recalled by Premiere Sales Group Due to Undeclared Active
The Issue: Marketed without an Approved NDA/ANDA: Products contain undeclared active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moonstruck Chocolates 9 piece Nuts & Chews Collection. The box Recalled by...
The Issue: Moonstruck Chocolates 9pc Nuts & Chews Collection product is recalled due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dimension Vista System (MG) Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Erroneous low results on a small number of reagent wells. There is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD CD3 (SK7) FITC Recalled by Becton, Dickinson and Company, BD Biosciences...
The Issue: Two lots of CD3 (SK7) FITC label contains an error in the Spanish Small text.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burn Relief¿ Recalled by O-Two Medical Technologies, Inc. Due to For lack of...
The Issue: For lack of evidence to validate effectiveness of sterilization dose, O-Two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amidate (Etomidate Injection Recalled by Hospira Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification(OOS)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultimate Herbal Slimcap Capsules Recalled by Fit Firm and Fabulous Due to...
The Issue: Marketed Without An Approved NDA/ANDA: product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Stryker Orthopaedics Recalled by Stryker Howmedica Osteonics Corp. Due to...
The Issue: Stryker is recalling various lots of the Trithion MIS Modular Distal Capture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 2.7MM/3.5MM VA-LCP Medial Distal Humerus Plates 10H/RT/186mm-...
The Issue: The 2.7MM/3.5MM VA-LCP Humerus Plates were found to be labeled incorrectly....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.