Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,475 recalls have been distributed to Minnesota in the last 12 months.
Showing 31261–31280 of 52,120 recalls
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P644) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P621) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-GP71) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N217) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N292) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P606) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P629) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N350) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P603) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N211) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N293) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Acumed Slide-Loc Anatomic Radial Head System is intended for Recalled by...
The Issue: The firm initiates a voluntary removal and discontinue marketing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10-1398M - SpF-PLUS Implantable Stimulator. Indicated as a spinal fusion...
The Issue: Zimmer Biomet is conducting a medical device field action for the SpF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10-1335M - SpF-XL IIB 2/DM Implantable Stimulator. Indicated as a Recalled...
The Issue: Zimmer Biomet is conducting a medical device field action for the SpF...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microfil Composite Instruments are packaged in an unsealed plastic sleeve...
The Issue: Microfil Composite Instruments were distributed with a sterile symbol on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shield and Protect Moisture Barrier Cream Recalled by Gentell, Inc Due to...
The Issue: GMP Deviations; product may not meet cGMP requirements
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol 20 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...
The Issue: CGMP deviations- Lack of Quality Assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol 12.5 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...
The Issue: CGMP deviations- Lack of Quality Assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol 10 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...
The Issue: CGMP deviations- Lack of Quality Assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol 22 mg pellet 99.5% Estradiol USP Recalled by Qualgen Due to CGMP...
The Issue: CGMP deviations- Lack of Quality Assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.