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. 2,517 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,517 in last 12 months

Showing 3498135000 of 53,342 recalls

FoodJuly 5, 2016· Newly Weds Foods Inc

Recalled Item: Bulk flour bland breader packaged into 15 Recalled by Newly Weds Foods Inc...

The Issue: Flour contaminated with E. coli O121 was used in the manufacuring of flour...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 5, 2016· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint¿ 500 v2.2.2A Software Upgrade Kit Recalled by Siemens...

The Issue: Some v2.2.2 upgrade kits include a dialysate mode which not cleared/approved...

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

Class III — Low RiskOngoing
Medical DeviceJuly 5, 2016· Branan Medical Corporation

Recalled Item: AmediCheck Instant Test Cup Recalled by Branan Medical Corporation Due to...

The Issue: Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug...

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

Class III — Low RiskOngoing
Medical DeviceJuly 5, 2016· Implant Direct Sybron Manufacturing, LLC

Recalled Item: RePlant¿ Angled Abutment Part Number 6050-52-60 Recalled by Implant Direct...

The Issue: Issue with design specification; oversized condition.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece Loaner Recalled by Zimmer Surgical Inc...

The Issue: Zimmer Biomet Surgical has received product complaints reporting that the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece w/o Hose Recalled by Zimmer Surgical Inc...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Handpiece Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 4, 2016· Zimmer Surgical Inc

Recalled Item: Zimmer¿ Air Dermatome II Width Plate Recalled by Zimmer Surgical Inc Due to...

The Issue: The surface coating applied to the device is blistering, peeling and...

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

Class II — Potential Health HazardOngoing
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Strawberry Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Blackberry Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Original Lemonade Recalled by Coca-Cola Company (The) Due to Foreign...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Watermelon Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 1, 2016· Circulatory Technology Inc

Recalled Item: The Better-Bladder With 14" ID tubing Recalled by Circulatory Technology Inc...

The Issue: Twisted or wrinkled balloon components which are considered a cosmetic...

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

Class III — Low RiskOngoing
Medical DeviceJuly 1, 2016· Circulatory Technology Inc

Recalled Item: The Bigger-Better-Bladder Recalled by Circulatory Technology Inc Due to The...

The Issue: The seal between the balloon and the housing may leak.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Sysmex America Inc

Recalled Item: Fluorocell PLT reagent Recalled by Sysmex America Inc Due to There is a...

The Issue: There is a potential that fluorescent platelet (PLT-F) and immature platelet...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 120 V Neptune 3 Rover Recalled by Stryker Instruments Div. of Stryker...

The Issue: Stryker initiated a voluntary recall of the 120 V Neptune 3 Rover on...

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

Class II — Potential Health HazardOngoing