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. 2,467 recalls have been distributed to Minnesota in the last 12 months.
Showing 32641–32660 of 52,120 recalls
Recalled Item: RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall...
The Issue: Product complaints indicated that the part and lot numbers on the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Active Articulation ArComXL Polyethylene Bearings Active Articulation...
The Issue: Product complaints indicated that the part and lot numbers on the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter Inc....
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN....
The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800. MDL Numbers: D222250 Recalled by GE OEC Medical Systems, Inc Due...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code:...
The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 6800 Recalled by GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OEC 9900 Elite mobile fluoroscopy system is designed to Recalled by GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium for Injection Recalled by Aurobindo Pharma USA Inc Due...
The Issue: Discoloration: Some vials were found to contain powder with a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIDAZOLAM INJECTION Recalled by Fresenius Kabi USA, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lite Creamy Alfredo Recalled by Berner Food & Beverage, LLC Due to Product...
The Issue: Product contaminated with spoilage bacteria, Enterobacter cloacae and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roasted Garlic Alfredo Recalled by Berner Food & Beverage, LLC Due to...
The Issue: Product contaminated with spoilage bacteria, Enterobacter cloacae and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Creamy Alfredo Recalled by Berner Food & Beverage, LLC Due to Product...
The Issue: Product contaminated with spoilage bacteria, Enterobacter cloacae and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Our Family Alfredo Recalled by Berner Food & Beverage, LLC Due to Product...
The Issue: Product contaminated with spoilage bacteria, Enterobacter cloacae and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Four Cheese Alfredo Recalled by Berner Food & Beverage, LLC Due to Product...
The Issue: Product contaminated with spoilage bacteria, Enterobacter cloacae and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker...
The Issue: The product was not functioning as intended. The ventilation to the patient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The AMM Recalled...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension AMM (DF119)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Ammonia Flex¿ reagent cartridge / AMM Dimension: The...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista AMM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Nellcor SpO2 Forehead Sensor Item Code: RS10 Recalled by Covidien...
The Issue: Labeling error: The label indicates the product is latex free, but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.