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. 2,576 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,576 in last 12 months

Showing 1642116440 of 29,286 recalls

Medical DeviceMay 8, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6)...

The Issue: The firm will be updating the Instructions for Use for the product. Current...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Zeiss, Carl Inc

Recalled Item: Cell Observer SD Recalled by Zeiss, Carl Inc Due to In certain eyepiece...

The Issue: In certain eyepiece configurations the laser shutter may not close...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Baxter Healthcare Corporation

Recalled Item: Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8)...

The Issue: The firm will be updating the Instructions for Use for the product. Current...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Wescam Inc

Recalled Item: MX-10 surveillance laser system Product Usage: The expected usage of...

The Issue: Product has a nominal ocular hazard distance (NOHD) that is longer than...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Stryker Sustainability Solutions

Recalled Item: Reprocessed HARMONIC Ace¿ +7 Recalled by Stryker Sustainability Solutions...

The Issue: Stryker Sustainability Solutions has received an increase in reports...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2018· Vyaire Medical

Recalled Item: AirLife Resuscitation Device Recalled by Vyaire Medical Due to An error in...

The Issue: An error in manufacturing of the AirLife Resuscitation Devices that has the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Aviva Plus Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm identified four US lots of test strips out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Inform II Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm has identified two lots of test strips that are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 7, 2018· Roche Diabetes Care, Inc.

Recalled Item: Accu-Chek Performa Test Strip Recalled by Roche Diabetes Care, Inc. Due to...

The Issue: The recalling firm has identified two lots of test strips that are out of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 5, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Sodium Slides Recalled by Ortho-Clinical Diagnostics Due to Potential...

The Issue: Potential for positively biased results

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Stryker GmbH

Recalled Item: Farabeuf Clamp for 3.5mm Screws PRO Recalled by Stryker GmbH Due to Laser...

The Issue: Laser etching which indicates whether the device is in compression or...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Vascular Solutions, Inc.

Recalled Item: Drainer(R) Centesis Catheters: (a) Recalled by Vascular Solutions, Inc. Due...

The Issue: The supplier of Drainer(R) centesis catheters notified Vascular Solutions,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Synthes (USA) Products LLC

Recalled Item: Synthes Torque Limiting Handle Recalled by Synthes (USA) Products LLC Due to...

The Issue: The adapter may demonstrate a degradation of function as the final products...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 4, 2018· Thermo Fisher

Recalled Item: remel SUPERPACK CS/ 500 SEG/FLASK Recalled by Thermo Fisher Due to Product...

The Issue: Product may fail performance testing for S aureus ATCC 43300.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Medtronic Neurosurgery

Recalled Item: Medtronic Clip Gun Magazines are packaged in individually sealed pouches...

The Issue: The packaging sterile barrier does not comply with the applicable packaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Ethicon Endo-Surgery Inc

Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...

The Issue: The devices may have been assembled with an internal component that may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...

The Issue: Ingress of fluids into the device can affect various electronic circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: P.R.O. Matt: (a) PROMATT PLUS 36 X 76 MATRESS Recalled by Joerns Healthcare...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2018· Ethicon Endo-Surgery Inc

Recalled Item: HARMONIC ACE Shears + Adaptive Tissue Technology Recalled by Ethicon...

The Issue: The devices may have been assembled with an internal component that may...

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

Class II — Potential Health HazardOngoing