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. 1,813 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
1,813 in last 12 months

Showing 3362133640 of 53,342 recalls

FoodOctober 10, 2016· Rosa Foods HQ

Recalled Item: Soylent Food Bars Recalled by Rosa Foods HQ Due to Rosa Foods is recalling...

The Issue: Rosa Foods is recalling Soylent Bar because a number of their customers have...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2016· Farm Country Cheese House, Inc.

Recalled Item: Hot Pepper Cheese Recalled by Farm Country Cheese House, Inc. Due to Farm...

The Issue: Farm Country Cheese House is conducting a voluntary recall of multiple vats...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2016· Farm Country Cheese House, Inc.

Recalled Item: White Cheddar Cheese Recalled by Farm Country Cheese House, Inc. Due to...

The Issue: Farm Country Cheese House is conducting a voluntary recall of multiple vats...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 10, 2016· Farm Country Cheese House, Inc.

Recalled Item: Marble Cheese Recalled by Farm Country Cheese House, Inc. Due to Farm...

The Issue: Farm Country Cheese House is conducting a voluntary recall of multiple vats...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2016· Farm Country Cheese House, Inc.

Recalled Item: White Cheddar Recalled by Farm Country Cheese House, Inc. Due to Farm...

The Issue: Farm Country Cheese House is conducting a voluntary recall of multiple vats...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 10, 2016· Farm Country Cheese House, Inc.

Recalled Item: Monterey Jack Cheese Recalled by Farm Country Cheese House, Inc. Due to Farm...

The Issue: Farm Country Cheese House is conducting a voluntary recall of multiple vats...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Unify Recalled by St Jude Medical Inc. Due to St Jude Medical is recalling...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Quadra Assura Recalled by St Jude Medical Inc. Due to St Jude Medical is...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2016· St Jude Medical Inc.

Recalled Item: Fortify VR Recalled by St Jude Medical Inc. Due to St Jude Medical is...

The Issue: St Jude Medical is recalling implantable cardiac defibrillator (ICD) and...

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

Class I — Serious Health HazardOngoing
FoodOctober 7, 2016· Kar Nut Products Company

Recalled Item: Fit & Active 100 Calorie Whole Almonds 7  0.63oz Recalled by Kar Nut...

The Issue: Walnuts undeclared on outer retail unit carton.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 7, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Advia Chemistry Calibrator For in vitro diagnostic use in the Recalled by...

The Issue: Siemens has confirmed that the DBIL_2 Assigned Calibrator Values (ACV)...

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

Class II — Potential Health HazardOngoing
DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: Persantine (dipyridamole USP) tablets Recalled by Boehringer Ingelheim...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 6, 2016· Boehringer Ingelheim Pharmaceuticals, Inc.

Recalled Item: DIPYRIDAMOLE Tablets USP Recalled by Boehringer Ingelheim Pharmaceuticals,...

The Issue: Presence of foreign tablets/capsules: 50 mg Persantine tablets were found in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Rotating Adult Craniotome Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Foot Control without Switches Recalled by The Anspach Effort, Inc. Due to...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Reciprocating MICRO SAW Recalled by The Anspach Effort, Inc. Due to Supplied...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Keyless Driver Product Usage: Pneumatic system Recalled by The Anspach...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 14cm QD Angle Attachment Product Usage: Pneumatic system Recalled by The...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: Electric Handpiece EM Hand Control Product Usage: Electric system Recalled...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 6, 2016· The Anspach Effort, Inc.

Recalled Item: 6.8cm Controlled Depth Attachment Product Usage: Pneumatic system Recalled...

The Issue: Supplied Directions for Use (DFU) did not contain a recommended service...

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

Class II — Potential Health HazardOngoing