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. 1,755 recalls have been distributed to North Carolina in the last 12 months.
Showing 45061–45080 of 54,363 recalls
Recalled Item: PERSONA The Personalized Knee System PS Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA" The Personalized Knee System UC Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Posterior Stabilized Tibial...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliSpace ECG Management System Recalled by Philips Medical...
The Issue: Philips IntelliSpace ECG (IECG) Management Systems that are importing Stress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System Constrained Tibial Articular Surface...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERSONA The Personalized Knee System CR Tibial Articular Surface Provisional...
The Issue: Reports of breakage of the Persona Knee Trial Articular Surface Provisionals...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTRACK250A Canaloplasty Microcatheter Kit Recalled by Ellex iScience, Inc....
The Issue: One lot may not have been properly sealed, resulting in a non-sterile device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parker Eclipse Probe Cover Recalled by Parker Laboratories, Inc. Due to...
The Issue: Parker Laboratories, Inc. received a report of an incorrect expiration date...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry A1c_3 CAL (Calibrator) for use on the ADVIA Chemistry...
The Issue: The ADVIA Chemistry Systems A1c_3 method may exhibit a percent bias of -9%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE Recalled by Angiodynamics, Inc....
The Issue: AngioDynamics became aware that Uni*Fuse Infusion Systems with Cooper Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MobileDiagnost wDR motorized portable diagnostic X-ray systems. Recalled by...
The Issue: Reports of unexpected movement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Select Kits (ASK) and Maximal Barrier Precautions Kits (CDC) Recalled...
The Issue: The component supplier recalled their 0.9% Sodium Chloride Injection USP BD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...
The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...
The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CHILDREN'S Q-PAP Recalled by Qualitest Pharmaceuticals Due to Superpotent...
The Issue: Superpotent Drug: Qualitest Pharmaceuticals is initiating a recall of three...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rifampin for Injection USP Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurity/Degradation Specification; high out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ZyGenerics ATENOLOL Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: Superpotent Drug: A complaint was reported by a pharmacist who stated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.