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. 2,783 recalls have been distributed to North Carolina in the last 12 months.
Showing 11301–11320 of 13,606 recalls
Recalled Item: Forever Beautiful BEE POLLEN Recalled by Enterprises, LLC Due to Marketed...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Forever Beautiful INFINITY Recalled by Enterprises, LLC Due to Marketed...
The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found product to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium in 0.9% Sodium Chloride Injection Recalled by Baxter...
The Issue: Subpotent Drug: Heparin raw material was found to have low potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Scrub Care Chlorhexidine Gluconate Solution Recalled by CareFusion 213, LLC...
The Issue: Does Not Meet Monograph: Chlorhexidine Gluconate Surgical Scrub Brush is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meropenem I.V. 1 g is supplied in 30 mL injection vials Recalled by Hospira...
The Issue: Defective Container: Glass vials may crack due to low (thin) out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mercaptopurine Tablets Recalled by Prometheus Laboratories Inc. Due to...
The Issue: Failed Dissolution Specifications: Product found to be out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Obagi Nu-Derm Clear Recalled by Obagi Medical Products Due to Labeling:...
The Issue: Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm Clear pre-labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Capsules Recalled by Aurobindo Pharma USA Inc Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Complaints of empty capsules received.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex 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: Cyproheptadine HCl Syrup (Cyproheptadine HCl Oral Solution Recalled by...
The Issue: Failed Impurities/Degradation Specifications : Out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex 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: Candesartan Cilexetil Tablets Recalled by Apotex 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: 1% LIDOCAINE HCl Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of particulate matter: A returned customer sample was evaluated and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Apotex 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: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.45% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose and 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Chloride in 5% Dextrose and 0.45% Sodium Chloride Injection...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Normosol-R pH 7.4 Multiple Electrolytes Injection Type 1 Recalled by Hospira...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...
The Issue: Lack of Assurance of Sterility: Potential of punctures through the overwrap...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.