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. 2,520 recalls have been distributed to Michigan in the last 12 months.
Showing 30261–30280 of 53,342 recalls
Recalled Item: Valero Baby Wedges with Crisp Coat UC Coating / 51049 (5 lb bags) Recalled...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags) Recalled by Penobscot...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Extra Large Coated Jo-Jo Wedges / 00048 (5 lb bags) Recalled by Penobscot...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System Recalled by...
The Issue: The firm has identified that a fitting in some Slidemaker Stainer units may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Recalled by...
The Issue: Software- scheduled A-QC analysis could initiate prior to a patient result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT 2¿ I.V. Gravity Flow Controller and STAT 2¿ Primary Recalled by ConMed...
The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT 2¿ I.V. Gravity Flow Needle-Free Controller Primary Administration Sets...
The Issue: Intravascular (I.V.) fluid administration sets are exhibiting inaccurate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Succinylcholine Chloride Recalled by Fagron Compounding Services LLC dba...
The Issue: Lack Of Assurance Of Sterility: voluntary recall initiated by the commercial...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LANTANA White Bean HUMMUS NET WT. 10 oz (283g) Recalled by House Of Thaller...
The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Marketside CLASSIC HUMMUS WITH PINE NUTS NET WT. 10 oz (283g) Recalled by...
The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: FRESH FOODS MARKET Artisan Humus Pine Nuts NET WT 10 oz (283g) Recalled by...
The Issue: The firm was notified by their ingredient supplier that the pine nuts may be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Max Implant System - Bone Tap for use with 7.0mm diameter Max Implant...
The Issue: An 8mm diameter bone tap was laser marked as 7mm diameter and was packed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100i Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp -...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 100 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS 300 Intra-Aortic Balloon Pump Recalled by Maquet Datascope Corp - Cardiac...
The Issue: The device failed to pump due to an electrical test failure code #58 (power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ibuprofen Tablets Recalled by Time-Cap Laboratories, Inc. Due to Presence of...
The Issue: Presence of foreign tablets/capsules: Ibuprofen Tablets USP, 600 mg bottles...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Injection USP Recalled by Alvogen, Inc Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Oral Solution Recalled by Tris Pharma Inc. Due to Defective...
The Issue: Defective container: Oral solution leaking from container.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.