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. 1,834 recalls have been distributed to Michigan in the last 12 months.
Showing 32621–32640 of 53,342 recalls
Recalled Item: GlipiZIDE Extended-release tablets Recalled by Amerisource Health Services...
The Issue: Failed dissolution specifications: Glipizide 2.5 mg ER Tablets exceeded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CycloSPORINE Capsules Recalled by Apotex Inc. Due to Failed...
The Issue: Failed Impurities/Degradations Specifications; out of specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artis zee Recalled by Siemens Medical Solutions USA, Inc Due to Failures can...
The Issue: Failures can result due to a component defect on Artis zee systems with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD System Controller The HeartWare Ventricular Assist System...
The Issue: Product recall of all HVAD Controllers currently on the market and to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transderm Scop (scopolamine) Transdermal System Recalled by Sandoz Inc Due...
The Issue: Labeling: Incorrect Instructions:outer carton contains the incorrect...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Q Care Continue Care Kit for the non-ventilated patient Recalled by Sage...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The expiration date of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mimvey Lo (estradiol and norethindrone acetate tablets USP) Recalled by Teva...
The Issue: Failed Impurities/Degradation Specifications: out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w...
The Issue: The stopcock was found to have punctures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Final Fit Software Version 1.11 and 1.12 Recalled by Nidek Inc Due to During...
The Issue: During treatment planning, the procedure was programmed with an unintended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micropuncture Check-Flo Performer Introducer Set Recalled by Cook Inc. Due...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriForce Peripheral Crossing Set Recalled by Cook Inc. Due to Devices using...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Hemostasis Assembly Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Set Recalled by Cook Inc. Due to Devices...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.