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. 2,563 recalls have been distributed to Michigan in the last 12 months.
Showing 24221–24240 of 53,342 recalls
Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to CGMP...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EMPOWR Locking Femoral Impactor Recalled by Encore Medical, Lp Due to The...
The Issue: The firm has received reports/complaints concerning the breakage of the tips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plain and Chromic Gut Absorbable Surgical Sutures Recalled by CP Medical Inc...
The Issue: Potential compromise of product sterility after routine monitoring for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US Endoscopy Padlock Clip defect closure system The Recalled by US Endoscopy...
The Issue: Potential esophageal laceration during a patient procedure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levoleucovorin Injection Recalled by Mylan Institutional Inc Due to Presence...
The Issue: Presence of Particulate Matter: particulate matter identified as copper salts
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dymista (azelastine hydrochloride and fluticasone propionate) Nasal Spray...
The Issue: Defective Container: Potential for broken glass in the neck area of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...
The Issue: Potentially comingled, resulting in the product in the box potentially not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGenTrabecular Metal Tibial Half Block Augment Recalled by Zimmer...
The Issue: Potentially comingled, resulting in the product in the box potentially not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Transseptal Needle Recalled by Cook Inc. Due to The products were...
The Issue: The products were manufactured without a back bevel on the needle tip. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Divalproex Sodium Extended-release Tablets Recalled by Dr. Reddy's...
The Issue: Failed Dissolution Specifications: Out of specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Semi-Rigid Suction Canister Recalled by Medline Industries Inc Due to...
The Issue: Potential for the Semi-Rigid canister lid to fragment during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use...
The Issue: Cepheid Xpert Respiratory Control Panel (Catalog #8199) has an reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl CD capsules Recalled by Valeant Pharmaceuticals North America...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cardizem CD (diltiazem HCl) capsules Recalled by Valeant Pharmaceuticals...
The Issue: Failed Dissolution Specifications: high out of specification results for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Velofix SA cervical cage Recalled by U&I CORP. Due to The vertical...
The Issue: The vertical dimensions of screw-hole position in some standalone cages...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Left - Product Usage: Recalled...
The Issue: Product mislabeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OMNIPORE Surgical Implant Petite Paranasal - Right - Product Usage: Recalled...
The Issue: Product mislabeling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.