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. 2,520 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,520 in last 12 months

Showing 3318133200 of 53,342 recalls

FoodDecember 7, 2016· All American Seasonings, Inc.

Recalled Item: French Onion Seasoning ASI. Product Code: T3933. 33 lb bags Recalled by All...

The Issue: Products have been recalled due to potential for Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 7, 2016· Cargill Cocoa & Chocolate, Inc.

Recalled Item: Wilbur Recalled by Cargill Cocoa & Chocolate, Inc. Due to Undeclared Milk

The Issue: Cargill Cocoa & Chocolate is recalling 50 lb. cartons of Wilbur B558...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 7, 2016· Novum Pharma, LLC

Recalled Item: Novacort Gel Sample Packets (2% hydrocortisone acetate Recalled by Novum...

The Issue: Subpotent Drug: Out of specification result for pramoxine hydrochloride

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 6, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT...

The Issue: A breach in the sterile packaging may have occurred resulting in potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2016· Stryker Sustainability Solutions

Recalled Item: Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT Recalled by...

The Issue: A breach in the sterile packaging may have occurred resulting in potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2016· Acumed LLC

Recalled Item: OPT Croutons is a synthetic bone substitute designed for the Recalled by...

The Issue: OPT Croutons, part number 65-0210-S, is recalled due to the result of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment...

The Issue: Reunion TSA Peg Alignment Sound broke during surgery.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Junction Box - 1104343 and 1193560 Recalled by Invacare Corporation Due to A...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 45 cm Product Code: HAL545 Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Bariatric Bed - BARPKG-IVC 1633 Recalled by Invacare Corporation Due to A...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 90 cm Product Code: HAL590 Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Foot Section - BAR5490IVC Recalled by Invacare Corporation Due to A quality...

The Issue: A quality issue with the junction box used in the bariatric bed junction...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Invacare Corporation

Recalled Item: Bariatric Bed - BAR600IVC Recalled by Invacare Corporation Due to The...

The Issue: The junction box used in the bariatric bed may emit sparks and result in a fire.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· Mckesson Medical Imaging

Recalled Item: McKesson Radiology 12.2 - Picture Archive Communication System (PACS)...

The Issue: Issue for customers that use an EMR login or legacy web URL login or legacy...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· BARD PERIPHERAL VASCULAR, INC

Recalled Item: Halo One 5F Introducer Sheath 10 cm 5 pack Product Recalled by BARD...

The Issue: Complaints of sheath separation, kinking, and/or tip damage during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· CareFusion 303, Inc.

Recalled Item: Alaris Pump Module Recalled by CareFusion 303, Inc. Due to During an...

The Issue: During an infusion, a false Air-in-Line (AIL) alarm would cause the infusion...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 2, 2016· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System The product is used to manage Recalled by...

The Issue: Edits to Particle field definition parameters may not be saved when the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2016· K2M, Inc

Recalled Item: K2M Special Connector Instruments (Special Connector Recalled by K2M, Inc...

The Issue: Instruments were developed without adequate consideration given to the need...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2016· Shire PLC

Recalled Item: Pentasa (mesalamine) Controlled-Release Capsules Recalled by Shire PLC Due...

The Issue: Presence of Foreign Tablets/Capsules; 500 mg capsules were found in bottles...

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

Class III — Low RiskOngoing
Refund
FoodDecember 2, 2016· Valley Milk Products

Recalled Item: Non Fat Dry Milk Recalled by Valley Milk Products Due to Potential...

The Issue: Products are recalled due to potential Salmonella contamination.

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

Class I — Serious Health HazardOngoing
Refund