Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,563 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,563 in last 12 months

Showing 2404124060 of 53,342 recalls

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 8, 2019· ulrich medical USA Inc

Recalled Item: ULRICH Torque Limiting Handle for use with a Set Screw Recalled by ulrich...

The Issue: Certain Torque Limiting Handles in the field are beyond their 3 year...

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

Class II — Potential Health HazardOngoing
DrugMarch 7, 2019· Boehringer Ingelheim Pharmaceuticals, Inc.

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.

Class III — Low RiskOngoing
Refund
DrugMarch 7, 2019· Medtech Products, Inc.

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.

Class II — Potential Health HazardOngoing
Refund
FoodMarch 7, 2019· GOOD KARMA FOODS INC

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.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2019· Becton Dickinson & Company

Recalled Item: BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25 Recalled by Becton...

The Issue: BD PAS received customer complaints indicating the absence of the bevel on...

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
Medical DeviceMarch 7, 2019· Stryker Corporation

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.

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

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.

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2019· Siemens Healthcare Diagnostics, Inc.

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.

Class II — Potential Health HazardOngoing