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 31401–31420 of 53,342 recalls
Recalled Item: Blephamide (sulfacetamide sodium and prednisolone acetate ophthalmic...
The Issue: Failed Impurities/Degradation Specifications: stability testing results did...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine HCI Injection Recalled by PAR Sterile Products LLC Due to...
The Issue: Crystallization: due to the presence of white, crystalline particulates,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FEM IM NAIL 14MMDX30CM LEFT Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TI Transport Monitor/Module Battery Pack Product Usage: intended for...
The Issue: Mindray has received two reports from outside the United States that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX II STD TUBE 130DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F IM NAIL 10MMDX48CM LG Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIBIAL I/M NAIL 15MMDX26CM Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FXII SC TUBE PLT 90DX16H Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Z NAIL PF 14MM X 46CM UNIV Z NAIL GT Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FEM IM NAIL 15MMDX30CM Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 BROAD SCP PLT 26-H STER Recalled by Zimmer Biomet, Inc. Due to Zimmer...
The Issue: Zimmer Biomet is initiating a field action for sterile-packaged implants...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Recalled...
The Issue: Potential sterile barrier breach
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to PEG kits have the potential for...
The Issue: PEG kits have the potential for one of the following defects: missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AbbVie PEG Recalled by AbbVie Inc. Due to PEG kits have the potential for...
The Issue: PEG kits have the potential for one of the following defects: missing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Minivelle (estradiol Transdermal System) 0.1 mg per day Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for peel force from the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acyclovir Tablets Recalled by Hetero USA Inc Due to Presence of Foreign...
The Issue: Presence of Foreign Substance: human hair melded into tablet.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Organic Veda brand Ginger Powder Recalled by Lords Organics Llc Due to...
The Issue: Lord Organics is recalling ginger powder because it has the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Resuscitation Recalled by Vyaire Medical Due to The mask component...
The Issue: The mask component on various lots of the resuscitation devices have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.