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. 2,576 recalls have been distributed to Michigan in the last 12 months.
Showing 22081–22100 of 53,342 recalls
Recalled Item: Clear Eyes Maximum Itchy Eye Relief Sidekick Floor Stand Display Recalled by...
The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25% Recalled by Medtech Products, Inc....
The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clear eyes REDNESS RELIEF (Glycerin 0.25% Recalled by Medtech Products, Inc....
The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clear eyes MAXIMUM REDNESS RELIEF (Glycerin 0.5% Recalled by Medtech...
The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clear Eyes Redness Relief Hand Pocket Pal Tray Display Recalled by Medtech...
The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clear eyes MAXIMUM ITCHY EYE RELIEF (Glycerin 0.25% Recalled by Medtech...
The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clear Eyes Maximum Redness and Itchy Eye Relief Sidekick Display Recalled by...
The Issue: CGMP Deviations: concerns regarding the sufficiency of Quality Assurance...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: da Vinci X Surgical System Surgical System Recalled by Intuitive Surgical,...
The Issue: The firm become aware of a potentially defective capacitors on circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Xi Surgical System Surgical System Recalled by Intuitive Surgical,...
The Issue: The firm become aware of a potentially defective capacitors on circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Surgical System Recalled by Intuitive Surgical, Inc. Due to The...
The Issue: The firm become aware of a potentially defective capacitors on circuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe OmniBed Carestation CS1 - Product Usage: The device can Recalled by...
The Issue: Fasteners potentially torqued to a value less than the specified value and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Urinalysis Control Level 2 (IVD) - Product Recalled by Randox...
The Issue: Analyte range for Leukocytes for use with the Siemens Multistix method is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo.CT software version VA48A_SP5.5 in the following SOMATOM computed...
The Issue: SOMATOM Definition Edge, SOMATOM Definition AS, SOMATOM Definition Flash...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrig ETF Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Push Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endintrak 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity of...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endintrak¿ 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.