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. 2,428 recalls have been distributed to Michigan in the last 12 months.
Showing 2621–2640 of 13,418 recalls
Recalled Item: Systane Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Racepinephrine Inhalation Solution Recalled by Mckesson Medical-Surgical...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Systane Zaditor Recalled by Mckesson Medical-Surgical Inc. Corporate Office...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pataday Recalled by Mckesson Medical-Surgical Inc. Corporate Office Due to...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Miralax (Polyethylene Glycol 3350) Recalled by Mckesson Medical-Surgical...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GenTeal Tears Recalled by Mckesson Medical-Surgical Inc. Corporate Office...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asthmanefrin Racephinephrine Inhalation Solution Bronchodilator Recalled by...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dakin's Solution Recalled by Mckesson Medical-Surgical Inc. Corporate Office...
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Telmisartan and Hydrochlorothiazide Tablets USP Recalled by Glenmark...
The Issue: Defective Container: Recall of these batches has been initiated due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Alcohol Prep Pads Recalled by Mckesson Medical-Surgical Inc....
The Issue: CGMP Deviations: products were stored outside the drug label specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrogen Peroxide Topical Solution USP Recalled by Vi-Jon, LLC Due to Cross...
The Issue: Cross Contamination With Other Products: Product is cross contaminated with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Aphrodisia Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Divalproex Sodium Delayed-Release Tablets Recalled by SUN PHARMACEUTICAL...
The Issue: Failed Dissolution Specifications: Failure occurred during routine stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product found to contain undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Capsules Recalled by Loud Muscle Science Due to Marketed...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Launch Sequence Euphoria Capsules Recalled by Loud Muscle Science Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Unapproved Drug based on label claims.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrogen Peroxide Topical Solution Recalled by Vi-Jon, LLC Due to Labeling:...
The Issue: Labeling: Label Mix-Up-The primary label on the front of the bottles have...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Customer complaints received for ripping patches...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.