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. 2,756 recalls have been distributed to North Carolina in the last 12 months.
Showing 11581–11600 of 54,363 recalls
Recalled Item: Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads Recalled by Acella...
The Issue: Subpotent drug: Out of specification for assay at the end-of-shelf-life...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenytoin Sodium Injection Recalled by Acella Pharmaceuticals, LLC Due to...
The Issue: Labeling: Not elsewhere classified; the product is being recalled because of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phenytoin Sodium Injection Recalled by Acella Pharmaceuticals, LLC Due to...
The Issue: Labeling: Not elsewhere classified; the product is being recalled because of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ACME Everything Bagel Smoked Salmon Net Wt. 4 OZ (113G) Recalled by Lidl US...
The Issue: Possible pathogen grown and toxin formation in Salmon products
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ACME Smoked Nova Salmon Net Wt. 4 OZ (113G) Recalled by Lidl US TRADING Due...
The Issue: Possible pathogen grown and toxin formation in Salmon products
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: iTotal Identity Impactor Handle Recalled by Conformis, Inc. Due to Loctite...
The Issue: Loctite thread locker (epoxy) may not have been applied to the screw that is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omnipod 5 Automated Insulin Delivery System Product catalog numbers:...
The Issue: The firm has become aware of an issue with the Omnipod 5 Controller where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Power-PRO 2 Recalled by Stryker Medical Division of Stryker Corporation Due...
The Issue: Cot may experience unintended motion due to damaged cables. Potential risk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phenoxybenzamine Hydrochloride Capsules Recalled by Par Formulations Private...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Neostigmine Methylsulfate Injection Recalled by Nephron Sterile...
The Issue: CGMP Deviations: Potential for cross contamination due to product carry over.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PF-Labetalol HCl Injection Recalled by Nephron Sterile Compounding Center...
The Issue: CGMP Deviations: Potential for cross contamination due to product carry over.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vivid S6 ultrasound. Used in ultrasound imaging and analysis in Recalled by...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S5 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S5 Ultrasound. Used in ultrasound imaging and analysis in Recalled by...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid i ultrasound. Marketed under the following 510(k) numbers: K033139...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid q ultrasound. Used in ultrasound imaging and analysis in Recalled by...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid q N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-CORE 2 Ti Core Recalled by NuVasive Inc Due to Potential that insert will...
The Issue: Potential that insert will be unable to disengage from the vertebral body...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid S6 N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vivid i N ultrasound. Not marketed in the US. Used Recalled by GE Medical...
The Issue: Potential for batteries that have not been replaced at 2 years, as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.