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. 1,022 recalls have been distributed to North Carolina in the last 12 months.
Showing 24841–24860 of 54,363 recalls
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diego Elite Turbinate Blades Bipolar Blade Recalled by Gyrus ACMI, Inc. Due...
The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Tibial Ankle Prosthesis Tray Recalled by Integra LifeSciences...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talar Dome Total Ankle Prosthesis Recalled by Integra LifeSciences Corp. Due...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Salto Talaris Tibial Total Ankle Prosthesis Tray Recalled by Integra...
The Issue: The Salto Talaris and Integra XT Revision implant labelling was found to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan Potassium USP Recalled by PD-Rx Pharmaceuticals, Inc. Due to CGMP...
The Issue: CGMP deviation: Product found to contain trace amounts of NMBA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PL Trader Joe Natural Creamer - Vanilla 12/32oz Recalled by GOOD KARMA FOODS...
The Issue: Product was recalled due to undeclared milk. The Contains statement does not...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mirapex (pramipexole dihydrochloride) Tablets Recalled by Boehringer...
The Issue: Failed Tablet/Capsule Specifications: identification of low weight tablets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Little Remedies New Baby Essentials Kit. Each kit contains 1 Recalled by...
The Issue: Incorrect/undeclared excipients: Kit carton bear incorrect labeling for two...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There were multiple issues identified in the system software which required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker High Flow Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker High Flow II Tube Set Recalled by Stryker Corporation Due to The...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Heated Tube Set with Real-Time Pressure Sensing (RTP) Recalled by...
The Issue: The heated tube sets were consistently leaking and detaching from the cassette.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray BCID Panel Recalled by BioFire Diagnostics, LLC Due to Potential...
The Issue: Increased risk of false positive Enterobacteriaceae and Escherichia coli...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime Recalled by Siemens Healthcare Diagnostics,...
The Issue: There were multiple issues identified in the system software which required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: There were multiple issues identified in the system software which required...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a Recalled by Topcon...
The Issue: When a patient is selected in the patient data and another patient is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.