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. 2,632 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,632 in last 12 months

Showing 1884118860 of 53,342 recalls

FoodJune 24, 2020· BUILT BRANDS LLC

Recalled Item: Toffee Almond Chocolate covered protein bars Recalled by BUILT BRANDS LLC...

The Issue: Products may be moldy prior to the end of the stated shelf life.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 24, 2020· BUILT BRANDS LLC

Recalled Item: S'Mores Chocolate covered protein bars Recalled by BUILT BRANDS LLC Due to...

The Issue: Products may be moldy prior to the end of the stated shelf life.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 24, 2020· BUILT BRANDS LLC

Recalled Item: Peanut Butter Chocolate covered protein bars Recalled by BUILT BRANDS LLC...

The Issue: Products may be moldy prior to the end of the stated shelf life.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 24, 2020· Beyond Better Foods Llc

Recalled Item: Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert Recalled by...

The Issue: Product may contain undeclared milk. Chocolate Peanut Butter ice cream may...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 24, 2020· DNA Genotek Inc.

Recalled Item: PrepIT Q2A Kit Recalled by DNA Genotek Inc. Due to Reagents were shipped to...

The Issue: Reagents were shipped to customers after the Use by data indicated on its...

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

Class III — Low RiskOngoing
Medical DeviceJune 24, 2020· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew T-F1X0 RCG Drill Pac Recalled by Smith & Nephew, Inc. Due to...

The Issue: The T-Fix sterile package contains only one sleeve instead of two, The...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 24, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite with software versions syngo.via VB30 or VB40...

The Issue: If the user modifies for any reason (e.g. reduction of artifacts) the...

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

Class II — Potential Health HazardOngoing
DrugJune 23, 2020· Itech 361 LLC

Recalled Item: All Clean Hand Sanitizer Recalled by Itech 361 LLC Due to Undeclared Methanol

The Issue: Chemical Contamination: Product contains undeclared methanol.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Radial Pink Recalled by Chengdu Ai Qin E-commerce Co., Ltd...

The Issue: Colored contact lenses were distributed without FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Sutter Medizintechnik GmbH

Recalled Item: Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re...

The Issue: The label on the cardbox and the blister show the correct symbols for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Radial Brown Recalled by Chengdu Ai Qin E-commerce Co., Ltd...

The Issue: Colored contact lenses were distributed without FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Black Starshine Recalled by Chengdu Ai Qin E-commerce Co.,...

The Issue: Colored contact lenses were distributed without FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Devil Red Recalled by Chengdu Ai Qin E-commerce Co., Ltd Due...

The Issue: Colored contact lenses were distributed without FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Diamonds Starlight Recalled by Chengdu Ai Qin E-commerce Co.,...

The Issue: Colored contact lenses were distributed without FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Flower Grey Recalled by Chengdu Ai Qin E-commerce Co., Ltd...

The Issue: Colored contact lenses were distributed without FDA clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 23, 2020· Chengdu Ai Qin E-commerce Co., Ltd

Recalled Item: TTDEYE (brand) Flower Brown Recalled by Chengdu Ai Qin E-commerce Co., Ltd...

The Issue: Colored contact lenses were distributed without FDA clearance.

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

Class II — Potential Health HazardOngoing
DrugJune 22, 2020· UVT INC

Recalled Item: Saniderm ADVANCED HAND SANITIZER Recalled by UVT INC Due to Undeclared Methanol

The Issue: Chemical Contamination: Product contains undeclared methanol.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 22, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Software versions syngo.CT VB20 or VB20_SP1 in the following systems:...

The Issue: Sporadic problems with the current software may result in scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2020· Biosense Webster (israel), Ltd.

Recalled Item: CARTO 3 System (Software Version V7.1.80) Recalled by Biosense Webster...

The Issue: Software defect may result in disapperance of tag sites during recalculation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2020· GE Healthcare, LLC

Recalled Item: CARESCAPE ONE Recalled by GE Healthcare, LLC Due to CARESCAPE ONE may not...

The Issue: CARESCAPE ONE may not provide visual and audible alarms for Ventricular...

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

Class II — Potential Health HazardOngoing