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. 2,537 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,537 in last 12 months

Showing 2078120800 of 29,286 recalls

Medical DeviceApril 28, 2016· CMP Industries, Llc

Recalled Item: IMPAK Liquid Acrylic Resin sold under the following labels: 1) Recalled by...

The Issue: Possible presence of foreign material (rust).

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 28, 2016· Excelsior Medical Corp

Recalled Item: Excelsior Disposable Syringe Heparin Lock Flush Recalled by Excelsior...

The Issue: Certain lots of Heparin Lock Flush, USP Syringes (5 ml Fill in 10 ml...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 27, 2016· Orthofix, Inc

Recalled Item: Firebird NXG Spinal Fixation System Set Screw Driver used to Recalled by...

The Issue: There is a possibility that the subject set screw driver could disengage...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2016· Greatbatch Medical

Recalled Item: Torque Limiting Handle: PRECIMED Recalled by Greatbatch Medical Due to...

The Issue: Greatbatch Medical has initiated a global Field Recall for Torque Limiting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2016· STERILMED, INC.

Recalled Item: Reprocessed Microline Scissor Tips intended to be used with a Recalled by...

The Issue: Sterlilmed is recalling all unexpired Scissor Tips because of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2016· Greatbatch Medical

Recalled Item: Torque Limiting Screwdriver: Greatbatch Medical Recalled by Greatbatch...

The Issue: Greatbatch Medical has initiated a global Field Recall for Torque Limiting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2016· Greatbatch Medical

Recalled Item: Torque Limiting Adapter: Torque Limiting Attachment Recalled by Greatbatch...

The Issue: Greatbatch Medical has initiated a global Field Recall for Torque Limiting...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2016· Greiner Bio-One North America, Inc.

Recalled Item: 4 ml FX Sodium Fluoride/Potassium Oxalate tube Recalled by Greiner Bio-One...

The Issue: The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT S(20) - 3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: The bracket that is used to lift the cover has bolts that were not welded in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph mCT-S(64) 4R Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: The bracket that is used to lift the cover has bolts that were not welded in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT S(20) - 3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: The bracket that is used to lift the cover has bolts that were not welded in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· GSK Consumer Healthcare

Recalled Item: Breathe Right Clear Recalled by GSK Consumer Healthcare Due to Some cartons...

The Issue: Some cartons used in the secondary packaging of Breathe Right Clear, Large,...

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

Class III — Low RiskOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT S(20) - 4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: The bracket that is used to lift the cover has bolts that were not welded in...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Toshiba American Medical Systems Inc

Recalled Item: Toshiba America Medical Systems Recalled by Toshiba American Medical Systems...

The Issue: It has been found that if the scan range extends beyond the maximum Field of...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2016· Volcano Corporation

Recalled Item: Volcano s5 Recalled by Volcano Corporation Due to Volcano has become aware...

The Issue: Volcano has become aware of an incompatibility issue between Impacted...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Acumedia Manufacturers, Inc.

Recalled Item: Tryptic Soy Agar Recalled by Acumedia Manufacturers, Inc. Due to light...

The Issue: light precipitate may form in prepared plates of Acumedia Tryptic Soy Agar...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow Edge-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing