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. 2,654 recalls have been distributed to Minnesota in the last 12 months.
Showing 7061–7080 of 52,120 recalls
Recalled Item: SmartPath to dStream for 1.5T Recalled by Philips North America Due to An...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T Conversion Recalled by Philips North America Due to An...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X Recalled by Philips North America Due to An incorrect...
The Issue: An incorrect electrical shock warning label may have been placed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VANCOmycin HCl PF 1.25g added to 0.9% Sodium Chloride 250 mL IV bag Recalled...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FentaNYL citrate PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VANCOmycin HCl PF 1.5g added to 0.9% Sodium Chloride 250 mL IV bag Recalled...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FentaNYL citrate PF Recalled by Denver Solutions, LLC DBA Leiters Health Due...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 20 mg per 250 mL 0.9% Sodium Chloride (80 mcg per mL)...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl 40 mg per 250 mL 0.9% Sodium Chloride (160 mcg per mL)...
The Issue: Superpotent Drug: semi-automated IV bag filling system can malfunction and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DELFLEX Peritoneal Dialysis Solution in Biofine container 1.5% Dextrose...
The Issue: Lack of Sterility Assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe Recalled by MRP,...
The Issue: The saline flush syringes may fail to meet USP criteria for stated sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Samsung Digital Diagnostic Mobile X-ray System Recalled by NeuroLogica...
The Issue: Mobile x-ray systems moving arm frame welding issue which presents the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bubble Sensor (.5720) Recalled by Maquet Medical Systems USA Due to The...
The Issue: The Bubble Sensor optional accessory to the CARDIOHELP-i extracorporeal life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardinal Health Monoject Recalled by Cardinal Health 200, LLC Due to...
The Issue: Cardinal Health is expanding their previous product correction actions to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.