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. 2,694 recalls have been distributed to Michigan in the last 12 months.
Showing 10301–10320 of 53,342 recalls
Recalled Item: Phenylephrine HCl 20 mg (80 mcg/mL) added to 0.9% Sodium Chloride 250 mL IV...
The Issue: CGMP DEVIATIONS
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chukar Cherries Cherry Bombs Bits 'n Pieces Recalled by Chukar Cherry...
The Issue: undeclared hazelnuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...
The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Recalled by Bio-Rad Laboratories, Inc. Due to Bio-Rad received...
The Issue: Bio-Rad received four customer complaints from 11/30/2022 to 12/21/2022 on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...
The Issue: Incorrect labeling; specifically, the product name, lot number and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath Recalled by...
The Issue: Incorrect labeling; specifically, the product name, lot number and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Lysis Beads Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neodent GM X 6mm Engaging Titanium Base Recalled by Preat Corp Due to...
The Issue: Engaging titanium base contains a dimensional condition that allows vertical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD with RVD Enhancer: a) 1 mL Recalled by Entopsis , Inc....
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis BCSNano (1mL) Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Support: a) 1 mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent RVD-RT Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Activator: a) 1.5mL Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCRopsis Reagent Buccal Recalled by Entopsis , Inc. Due to Presence of...
The Issue: Presence of misleading label statements on the product label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPerfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2D Perfusion Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to There...
The Issue: There are technical issues related to signal generation and processing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a...
The Issue: Battery leakage can cause corrosion to the metal enclosure near the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US Recalled by Mead Johnson & Company Due...
The Issue: Reckitt, a producer of nutrition products, announced today that out of an...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DIBUCAINE 1% HEMORRHOIDAL OINTMENT Recalled by Akron Pharma, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Tablets Recalled by Sciegen Pharmaceuticals Inc Due to Presence...
The Issue: Presence of Foreign Tablets/Capsules: Pharmacist reported presence of some...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.