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. 2,505 recalls have been distributed to Minnesota in the last 12 months.
Showing 22241–22260 of 52,120 recalls
Recalled Item: PROBAR MEAL Original Trail Mix Recalled by Probar LLC Due to Undeclared Milk
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROBAR MEAL Peanut Butter Chocolate Chip Recalled by Probar LLC Due to...
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROBAR MEAL Chocolate Coconut Recalled by Probar LLC Due to Undeclared Milk
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: DaVinci Laboratories of Vermont Omega 3-1 Recalled by FoodScience...
The Issue: Dietary supplement mislabeled, undeclared allergen.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PROBAR MEAL Wholeberry Blast Recalled by Probar LLC Due to Undeclared Milk
The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...
The Issue: code 7-102 Liquid Sensor Error
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...
The Issue: The action has been initiated to address reports of burst balloons which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...
The Issue: The action has been initiated to address reports of burst balloons which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Prisma magnetic resonance diagnostic devices Model #10849582...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Skyra magnetic resonance diagnostic devices Model # 10432915...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914...
The Issue: Potential of an open port in the quench venting system when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...
The Issue: The action has been initiated to address reports of burst balloons which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards SAPIEN 3 Ultra Transcatheter Heart Valve System (SAPIEN 3 Recalled...
The Issue: The action has been initiated to address reports of burst balloons which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gablofen (baclofen injection) Recalled by Piramal Critical Care, Inc. Due to...
The Issue: Failed Impurities/Degradation Specification -This recall is being initiated...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) II - Product Usage: Recalled by Becton,...
The Issue: The recalling firm confirmed that BD FACS Sample Prep Assistant (SPA) II and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) III - Product Usage: Recalled by Becton,...
The Issue: The recalling firm confirmed that SPA II and III users may encounter probes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACS Sample Prep Assistant (SPA) II Upgrade - Product Recalled by Becton,...
The Issue: The recalling firm confirmed that SPA II and III users may encounter probes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visualase Cooled Laser Applicator System Tubing Set kits Product numbers:...
The Issue: The firm received complaints on the saline tubing of Visualase Cooled Laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GRIPPER Needles sold individually. Labeled as the following item...
The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.