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. 2,666 recalls have been distributed to Michigan in the last 12 months.
Showing 14541–14560 of 53,342 recalls
Recalled Item: Extra Strength Headache (acetaminophen 250 mg Recalled by Medique Products...
The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medique Pain-Off (Acetaminophen 250 mg Recalled by Medique Products Due to...
The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: kleantouch HAND SANITIZER (ethyl alcohol 70%) Recalled by Valisa MFG LLC Due...
The Issue: Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...
The Issue: There is a potential for abnormal (non-sigmoidal) amplification curves.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...
The Issue: There is a software issue associated with the ability to properly complete a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is an issue...
The Issue: There is an issue with the installation of updated camera firmware on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CTx7 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CariFree sample boxes Recalled by Dental Alliance Holdings LLC Due to...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx12 5000 Kit which contains 3 boxes of CariFree CTx4 Recalled by Dental...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx21 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CariFree CTx4 GEl 5000 1.1% Neutral Sodium Fluoride Mint Recalled by Dental...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx36 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CTx26 Kit Recalled by Dental Alliance Holdings LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: Product contains less Sodium Fluoride than listed on product...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate Oral Solution 100 mg per 5 mL (20 mg/mL) 30 mL bottles...
The Issue: Labeling: Missing Label
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone Hydrochloride Oral Solution Recalled by Akorn, Inc. Due to...
The Issue: Labeling: Missing Label
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Veklury (remdesivir) for injection Recalled by Gilead Sciences, Inc. Due to...
The Issue: Presence of Particulate Matter: investigation into a customer complaint...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BUBS Naturals Fountain of Youth Formula Recalled by Slayer Forever, LLC dba...
The Issue: Supplement contains undeclared milk from MCT oil powder ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ImagePilot Versions 1.92 and 1.93-software primarily facilitates processing...
The Issue: lmagePilot versions 1.92 and 1.93 paired with an AeroDR or Momentum Panel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.