Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,503 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,503 in last 12 months

Showing 1426114280 of 27,833 recalls

Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Tibial Total Ankle Prosthesis Tray Recalled by Integra LifeSciences Corp....

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Diego Elite Malleable Recalled by Gyrus ACMI, Inc. Due to Olympus Diego...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Tibial Total Ankle Prosthesis Tray Recalled by Integra LifeSciences Corp....

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Tibial Total Ankle Prosthesis Tray Recalled by Integra LifeSciences Corp....

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Gyrus ACMI, Inc.

Recalled Item: Olympus Diego Elite Console MDCONS 100 Recalled by Gyrus ACMI, Inc. Due to...

The Issue: Olympus Diego Elite Consoles may inadvertently permit activation of the RF...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2019· Integra LifeSciences Corp.

Recalled Item: Salto Talaris Recalled by Integra LifeSciences Corp. Due to The Salto...

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Stryker Corporation

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.

Class II — Potential Health HazardOngoing