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. 2,452 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,452 in last 12 months

Showing 3556135580 of 52,120 recalls

FoodApril 21, 2016· CSM Bakery Products NA

Recalled Item: Copack Wht/Yelcupcakebase 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.

Class II — Potential Health HazardOngoing
Refund
FoodApril 21, 2016· CSM Bakery Products NA

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.

Class II — Potential Health HazardOngoing
Refund
FoodApril 21, 2016· CSM Bakery Products NA

Recalled Item: 7-Eleven Sugar Cookie 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.

Class II — Potential Health HazardOngoing
Refund
FoodApril 21, 2016· CSM Bakery Products NA

Recalled Item: 7-Eleven Variety Cookie 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.

Class II — Potential Health HazardOngoing
Refund
FoodApril 21, 2016· Vitalicious Acquisition

Recalled Item: VitaTops Apple Crumb Recalled by Vitalicious Acquisition Due to Undeclared Milk

The Issue: The affected lots of VitaTops Apple Crumb contain undeclared milk.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 21, 2016· Musculoskeletal Transplant Foundation, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Draeger Medical, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

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.

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

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.

Class II — Potential Health HazardOngoing
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Norepinephrine 16 mg added to 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.

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Oxytocin 10 Units added to Lactated Ringers in a 500 mL lntravia bag...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Norepinephrine Bitartrate 8mg Added to 5% Dextrose 250 mL bag Recalled by...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Diltiazem HCI 250 mg in 5% Dextrose Recalled by Pharmakon Pharmaceuticals,...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Bupivacaine HCI 0.125% 50 mL fill in a 60 mL syringe Recalled by Pharmakon...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Lidocaine 2% Recalled by Pharmakon Pharmaceuticals, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: Epinephrine (PF) 10mcg/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.

Class II — Potential Health HazardOngoing
Refund
DrugApril 20, 2016· Pharmakon Pharmaceuticals, Inc.

Recalled Item: HYDROmorphone HCI 1mg/mL in 0.9% Sodium Chloride 30 mL fill Recalled by...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund