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. 994 recalls have been distributed to Michigan in the last 12 months.
Showing 34981–35000 of 53,342 recalls
Recalled Item: FE Green Bell Pepper Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE RedBell Pepper 339 Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE Green Bell Pepper 338 Recalled by QualiTech, Inc Due to Potential E. coli...
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FE Maple Recalled by QualiTech, Inc Due to Potential E. coli Contamination
The Issue: QualiTech has been notified by a supplier that they received material with...
Recommended Action: Do not consume. Return to store for a refund or discard.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...
The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: OPTICAL BIOMETER AL-Scan: Software Version: 1.09 and earlier. Ophthalmic:...
The Issue: Nidek Inc. received information from our manufacturer NIDEK CO. Japan that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
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.
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.