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. 2,742 recalls have been distributed to Michigan in the last 12 months.
Showing 2921–2940 of 53,342 recalls
Recalled Item: Walgreens Maximum Strength Tinted Acne Treatment Cream 10% Benzoyl...
The Issue: Chemical contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD PYXIS MEDBANK (Name Recalled by CareFusion 303, Inc. Due to Users trying...
The Issue: Users trying to restock a single bin location of an automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD 4 Fr Single-Lumen PowerPICC Catheters Recalled by Bard Access Systems,...
The Issue: Catheters indicated for short-or-long term access to the central venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower Recalled by CareFusion...
The Issue: Due to a software bug, automated dispensing cabinet is unable to calculate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Revised C Reactive Protein (RCRP) Recalled by Siemens Healthcare...
The Issue: Incorrect software flagging may occur for the assay that may potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Pyxis MedBank CUBIE Replenishment Station Product / Material ID Recalled...
The Issue: Due to a software issue, when attempting to restock the automated dispensing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Nerve Monitoring System: CONSOLE NIM4CM01 NIM 4.0 Recalled by...
The Issue: Nerve Monitoring System with certain software versions has potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for collimator to fall as a result of incorrect installation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet VH-3010 Power Supply. Used to deliver power to the Recalled by Maquet...
The Issue: Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DXR System Recalled by Philips North America Llc Due to Potential...
The Issue: Potential for collimator to fall as a result of incorrect installation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TLX/TLC SP Guided Implant Driver Recalled by Straumann USA LLC Due to The...
The Issue: The devices are missing the laser marked depth markings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine D/R Recalled by Direct Rx Due to CGMP Deviations: Presence of...
The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine D/R Recalled by Direct Rx Due to CGMP Deviations: Presence of...
The Issue: CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sofosbuvir and Velpatasvir Recalled by ASEGUA THERAPEUTICS LLC Due to...
The Issue: Defective Container: blister packs not properly sealed resulting in tablets...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection Recalled by Exela Pharma Sciences LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Super-Potent Drug: Out of specification potency results were obtained.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets 60 mg Recalled by Slate Run Pharmaceuticals...
The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...
The Issue: Super-Potent Drug: Out of specification potency results were obtained.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cinacalcet Hydrochloride Tablets 30 mg Recalled by Slate Run Pharmaceuticals...
The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP Recalled by Ethicon Endo...
The Issue: Identified curing issues with the silicone during the needles manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.