Product Recalls in New York
Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,956 recalls have been distributed to New York in the last 12 months.
Showing 25781–25800 of 55,896 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: Abbott Alinity ci-series System Control Module software version 2.5.1...
The Issue: Potential performance issues in the Alinity-ci software version 2.5.1
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: 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: 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.