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. 2,742 recalls have been distributed to Michigan in the last 12 months.
Showing 2701–2720 of 53,342 recalls
Recalled Item: Mexican Street Corn Soup Recalled by Request Foods Incorporated Due to...
The Issue: Potential contamination with foreign material (wood)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Beecher's Street Corn Recalled by Request Foods Incorporated Due to Foreign...
The Issue: Potential contamination with foreign material (wood)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Marketside brand celery stick. Net wt. 1.6 OZ. (45g) Recalled by Duda Farm...
The Issue: Product tested positive for Listeria Monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KliniTray Platte Faxitron Recalled by Klinika Mdical Gmb Due to Potential...
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KliniTray. KlinioTray. Tissue resection margin examination board/small....
The Issue: Potential for microbial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSPIRA AIR BALLOON DILATION SYSTEM 10x40 Recalled by Integra LifeSciences...
The Issue: Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Pro...
The Issue: Preset treatment parameters are not consistently being used in accordance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Label: FROZEN CHOPPED CILANTRO Recalled by Supherb Farms Due to Foreign...
The Issue: Potential contamination with foreign objects.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Label: IQF CILANTRO LARGE Recalled by Supherb Farms Due to Foreign Object...
The Issue: Potential contamination with foreign objects.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Zydus Pharmaceuticals (USA)...
The Issue: CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Posterior Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due to The...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enhanced Verify Evaluation Handset (CFN HH90130FA) Recalled by Medtronic...
The Issue: Evaluation handsets may not be able to communicate with the neurostimulator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Distal Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Shaped Femoral Augment Recalled by Waldemar Link GmbH & Co. KG (Mfg Site)...
The Issue: The device was delivered with a preassembled Femoral Augment screw that was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGEC 2 Rod Recalled by Globus Medical, Inc. Due to Devices for the affected...
The Issue: Devices for the affected lot were not assembled according to product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...
The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...
The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Amerisource Health Services LLC...
The Issue: Lack of assurance of sterility. Bacterial contamination detected in some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment Recalled by Preat...
The Issue: Due to manufacturing issues, abutment products were manufactured with screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.