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. 2,673 recalls have been distributed to Michigan in the last 12 months.
Showing 13041–13060 of 53,342 recalls
Recalled Item: INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 Recalled by Smith &...
The Issue: Right nails were anodized, marked, and labelled as left nails and vice versa
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Erythromycin Topical Gel USP Recalled by McKesson Corporation dba McKesson...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Halobetasol Propionate Ointment 0.05% Net Wt. Recalled by McKesson...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Prilocaine Cream USP Recalled by McKesson Corporation dba McKesson...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betamethasone Dipropionate Ointment USP Recalled by McKesson Corporation dba...
The Issue: CGMP Deviations: all products within expiry are being recalled because the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version...
The Issue: Due to interference with the Live Listen feature of hearing aid or AirPods,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium Firm PVC Thoracic Catheter 28French-Intended to facilitate the...
The Issue: Mismatch between the expiration date on the sterile barrier pouch and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PX200 Emergency Relief Bed Recalled by Oakworks Inc Due to Product label was...
The Issue: Product label was printed without the UDI number and warning label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oakworks Bed (Emergency Field Bed) Recalled by Oakworks Inc Due to The...
The Issue: The warning label was printed with the incorrect weight capacity. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 15 Liters Drain Bag Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 Recalled by Baxter Healthcare Corporation Due to Certain Peritoneal...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APD Drain Manifold Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locking Cap for PD Catheter Adapter Recalled by Baxter Healthcare...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5 Prong Manifold Set (with Luer Connectors) Recalled by Baxter Healthcare...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Effluent Sample Bag Recalled by Baxter Healthcare Corporation Due to Certain...
The Issue: Certain Peritoneal Dialysis product codes do not have FDA regulatory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus URETERO-RENO FIBERSCOPE Model: URF-P6R Recalled by Olympus...
The Issue: Incorrect adhesive used to secure the diopter ring and nameplate ring....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus URETERO-RENO FIBERSCOPE Model: URF-P6 Recalled by Olympus...
The Issue: Incorrect adhesive used to secure the diopter ring and nameplate ring....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus CYSTONEPHROFIBERSCOPE Model: CYF-5 Recalled by Olympus Corporation...
The Issue: Incorrect adhesive used to secure the diopter ring and nameplate ring....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus235- Proton Therapy System: to produce and deliver a proton Recalled...
The Issue: First layer of Uniform Scanning treatment fields is sometimes irradiated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.