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. 1,014 recalls have been distributed to Minnesota in the last 12 months.
Showing 35561–35580 of 52,120 recalls
Recalled Item: BM Westco 1440 Yst Rds Donut Base Recalled by CSM Bakery Products NA Due to...
The Issue: Undeclared allergen; Peanut Protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Brill Choco Cream Cake Base Recalled by CSM Bakery Products NA Due to...
The Issue: Undeclared allergen; Peanut Protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Yeast Roll Mix Recalled by CSM Bakery Products NA Due to Undeclared Allergen
The Issue: Undeclared allergen; Peanut Protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BM Westco Sup-R-Roll Donut Mix Recalled by CSM Bakery Products NA Due to...
The Issue: Undeclared allergen; Peanut Protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Buffets Corn Muffin Mix Recalled by CSM Bakery Products NA Due to Undeclared...
The Issue: Undeclared allergen; Peanut Protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and...
The Issue: Operators noticed unwanted release of evaporating anesthetic agent at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...
The Issue: Instructions for use booklet may puncture the outer Tyvek lid.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant...
The Issue: AFT Diverted Tubes are being recalled due to a customer complaint involving...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate 5 mcg/mL & Bupivacaine 0.06% in 0.9% Sodium Chloride...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCI 0.2mg/ml in 0.9% Sodium Chloride Recalled by Pharmakon...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate 2 mcg/mL/Ropivacaine HCI 0.2% injection in 0.9% Sodium...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketamine 2 mg/mL in 0.9% Sodium Chloride 30 mL fill Recalled by Pharmakon...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUCONPO CAPSULE Recalled by Murray International Trading Co., Inc. Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Products marked as dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ephedrine Sulfate 5 mg/mL in 0.9% Sodium Chloride Recalled by Pharmakon...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Morphine Sulfate (Preserved) 2mg/mL in 0.9% Sodium Chloride 50 mL Recalled...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate 2mcg/mL & 0.2% Ropivacaine HCI in 0.9% Sodium Chloride...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.