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. 2,689 recalls have been distributed to Michigan in the last 12 months.
Showing 12201–12220 of 53,342 recalls
Recalled Item: Aspirin and Extended-Release Dipyridamole Capsules Recalled by Glenmark...
The Issue: Failed Tablet/Capsule Specification : Capsule breakage
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Orthex External Fixation Wire Sharp Bayonet 1.8 x 400 mm Model: K400-18BN...
The Issue: Manufacturing variance near transition of tip is increasing the likelihood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARTO VIZIGO 8.5F Bi-Directional Guiding Sheath Recalled by Biosense...
The Issue: Outside packaging for a device indicated for introducing cardiovascular...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sklar Instruments IV Cath Dressing Tray Cs/25 Re-Order Number: 96-1708...
The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wolf Pak Premium Dressing Change Kit with GuardVA and Statlok Recalled by...
The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wolf Pak Premium Dressing Change Kit with Statlock CS/30 Recalled by Trinity...
The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wolf-Pak Premium Dressing Kit with GuardVA Cs/30 Recalled by Trinity...
The Issue: Kits mislabeled as latex-free, the packaging for component 94-7002...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDLINE MICRO-KILL GERMICIDAL BLEACH WIPES Recalled by MEDLINE INDUSTRIES,...
The Issue: stability failure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATTUNE Measured Sizing and Rotation Guide-to size the femur and Recalled by...
The Issue: Manufactured with a Galvanized High Carbon Steel spring instead of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SX-One MicroKnife Recalled by SONEX HEALTH LLC Due to Potential of dull blade
The Issue: Potential of dull blade
Recommended Action: Stop using. Contact the manufacturer or your 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: BIOPHEN UFH Control Plasma Recalled by Aniara Diagnostica LLC Due to...
The Issue: Incorrect product labeling was included in the package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist Device (HVAD) System Batteries Recalled by...
The Issue: Battery performance issues. Battery electrical faults render it unable to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Iron_2 (Iron_2) is for in vitro diagnostic use Recalled by...
The Issue: Falsely Elevated Atellica CH Microalbumin_2 (¿ALB_2) Results due to Reagent...
Recommended Action: Stop using. Contact the manufacturer or your 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 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: 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 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 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.