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. 2,489 recalls have been distributed to Minnesota in the last 12 months.
Showing 24941–24960 of 52,120 recalls
Recalled Item: StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation...
The Issue: An incorrect display of the Biopsy Depth Gauge graphical representation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica Sample Handler Prime. In vitro diagnostic testing of clinical...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH 930 Analyzer. In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer. In vitro diagnostic testing of clinical Recalled...
The Issue: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCEA ASV Yellow Microbore Recalled by Becton Dickinson & Company Due to The...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCEA Kit ASV Yellow Stripe Microbore Recalled by Becton Dickinson & Company...
The Issue: The products have the potential to leak between the connection of the male...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prevacid 24HR (Lansoprazole) delayed-release capsules Recalled by...
The Issue: CGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Injection in 5% Dextrose Recalled by Baxter Healthcare...
The Issue: Superpotent Drug: High out of specification results for levofloxacin...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine 1% + Epinephrine 1:100 Recalled by RXQ Compounding LLC Due to...
The Issue: Subpotent drug: During testing of the retention sample, the firm discovered...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PRO-DEX Surgical Driver Battery Pack PDBP-001 Series PRO-DEX Battery Pack...
The Issue: Visual particulates within a battery Tyvek pouch. The battery is provided...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 365 Everyday Value Brand White Corn Chips Recalled by Whole Foods Market Due...
The Issue: Product may contain undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Zilver 635 Biliary Stent 14mm x 60mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver Biliary 518 Stent 5mm x 60mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 518 Biliary Stent 4mm x 30mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 518 Biliary Stent 5mm x 40mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 635 Biliary Stent 12mm x 80mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 518 Biliary Stent 5mm x 20mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 635 Biliary Stent 5mm x 40mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 635 Biliary Stent 4mm x 80mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zilver 518 Biliary Stent 4mm x 60mm Recalled by Cook Medical Incorporated...
The Issue: The instruction for use detail, with respect to removal of the delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.