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.
Showing 19241–19260 of 53,342 recalls
Recalled Item: A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM PROXIMAL HUMERUS PLATE TEMPLATE...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK GUIDE SLEEVE 2.7MM...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE LEFT 14 HOLE 234MM...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE RIGHT 14 HOLE 227MM...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM HIGH PLATE RIGHT 7 HOLE 140MM...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.L.P.S.¿ PROXIMAL HUMERUS PLATING SYSTEM LOW PLATE LEFT 14 HOLE 227MM...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet 6.5 Cannulated Screw Tap - Bone fixation screw Recalled by Biomet Due...
The Issue: Distributed to the field without having completed design history files or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Doxycycline Hyclate Tablets USP Recalled by West-Ward Columbus Inc Due to...
The Issue: Failed dissolution specification: The dissolution test at the 24 month time...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethacrynic Acid Tablets USP Recalled by West-Ward Columbus Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of Specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MOL3655 Simplexa VZV Swab Direct - Product Usage: is intended Recalled by...
The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOL2150 Simplexa HSV 1&2 Direct -CSF -Genital Swab -Cutaneous / Recalled by...
The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOL3650 Simplexa VZV Direct - Product Usage: is intended for Recalled by...
The Issue: Due to a software malfunction in the Multi Assay Suite, there is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity C Recalled by Abbott Gmbh & Co. KG Due to There is a potential to...
The Issue: There is a potential to generate incorrect patient results for the following...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Type S Extension For use with Varian Recalled by Med Tec Inc Due to...
The Issue: Potential for disengagement of the Varian Style Type-S Extension during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Confida Expandable Sheath Recalled by Medtronic Vascular Galway...
The Issue: Increased risk of events associated with vascular complications (bleeding,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Cannabidiol (CBD) + Curcumin 50mg/mL Recalled by BIOTA Biosciences...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Curcumin 50mg/mL Recalled by BIOTA Biosciences LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Curcumin Recalled by BIOTA Biosciences LLC Due to Lack of Assurance...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Cannabidiol (CBD) 4mg/mL Recalled by BIOTA Biosciences LLC Due to...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Cannabidiol (CBD) 50mg/mL Recalled by BIOTA Biosciences LLC Due to...
The Issue: Lack of Assurance of Sterility and Marketed without an approved NDA/ANDA:...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.