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. 2,424 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,424 in last 12 months

Showing 5210152120 of 53,342 recalls

DrugJune 27, 2012· Hospira Inc.

Recalled Item: Carboplatin Injection Recalled by Hospira Inc. Due to The affected lots of...

The Issue: The affected lots of Carboplatin Injection, Cytarabine Injection,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 27, 2012· Hospira Inc.

Recalled Item: Cytarabine Injection Recalled by Hospira Inc. Due to The affected lots of...

The Issue: The affected lots of Carboplatin Injection, Cytarabine Injection,...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJune 27, 2012· Standard Process, Inc.

Recalled Item: SP Standard Process Recalled by Standard Process, Inc. Due to Potential...

The Issue: Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJune 27, 2012· Standard Process, Inc.

Recalled Item: SP Standard Process Recalled by Standard Process, Inc. Due to Potential...

The Issue: Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJune 27, 2012· Standard Process, Inc.

Recalled Item: Standard Process Recalled by Standard Process, Inc. Due to Potential...

The Issue: Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 27, 2012· Mar Cor Purification

Recalled Item: Mar Cor Purification CWP Reverse Osmosis System. Models 101 Recalled by Mar...

The Issue: There exists a potential situation with the crimp connection at the pump...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· KCI USA, Inc.

Recalled Item: RotoRest Delta Kinetic Therapy System INDICATIONS: Treatment and prevention...

The Issue: The firm is initiating a voluntary medical device correction for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair. The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Stryker Medical Division of Stryker Corporation

Recalled Item: Powered Mobility Offers Versatility (M¿V)TM Chair. The Powered MOV Chair...

The Issue: Paramed Corporation (d/b/a, Descent Control Systems), a manufacturer and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Perkinelmer

Recalled Item: Perkin Elmer Genetic Screening Processor (GSP) Product Code: 2021-0010...

The Issue: Contamination from GSP Shaker unit results in decreased signal activity of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2012· Smiths Medical ASD, Inc.

Recalled Item: Smiths Medical HOTLINE 3 Blood and Fluid Warmer Recalled by Smiths Medical...

The Issue: HOTLINE 3 Blood and Fluid Warmer( Reorder No. HL-390 ) disposable is not...

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

Class II — Potential Health HazardOngoing
DrugJune 26, 2012· Ben Venue Laboratories Inc

Recalled Item: Vecuronium Bromide for Injection Recalled by Ben Venue Laboratories Inc Due...

The Issue: Presence of Particulate Matter

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 26, 2012· GE Healthcare, LLC

Recalled Item: GE Giraffe and Panda T-Piece Resuscitation System labeled ***T-Piece...

The Issue: Disposable T-Piece circuits used with resuscitation systems are unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 26, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential issue due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***Press FT***2.6 w/ One #2 (5 metric) Hi-Fi***Suture Recalled by Linvatec...

The Issue: Linvatec Corporation DBA ConMed Linvatec in Largo, FL is recalling Press FT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: NP211H***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO Recalled by...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***PressFT***2.1 w/ One #2 (5 metric)...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2012· Linvatec Corp. dba ConMed Linvatec

Recalled Item: "***PressFT***2.6 w/ Two #1 (4 metric)...

The Issue: Linvatec Corporation dba ConMed Linvatec in Largo, FL is recalling PressFT...

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

Class II — Potential Health HazardOngoing