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. 2,475 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,475 in last 12 months

Showing 3144131460 of 52,120 recalls

DrugApril 6, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Methylprednisolone Acetate 40 mg/mL Recalled by Isomeric Pharmacy Solution,...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Phenylephrine 2.5% Recalled by Isomeric Pharmacy Solution, LLC Due to Lack...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 6, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Methylprednisolone Acetate 80 mg/mL Recalled by Isomeric Pharmacy Solution,...

The Issue: Lack of Assurance of Sterility: due to concerns with production processes...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 6, 2017· Merge Healthcare, Inc.

Recalled Item: Fellows "Mighty 8" Power strip (Part Number 04175-0008) and TrippLite...

The Issue: Merge is conducting a hardware recall (replacement) of Fellows "Mighty 8"...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2017· Bausch & Lomb Surgical, Inc.

Recalled Item: SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for Recalled...

The Issue: Complaints concerning kinked haptics that were occurring during lens delivery.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2017· PEROUSE MEDICAL

Recalled Item: DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE Recalled by PEROUSE...

The Issue: Complaints regarding broken blister.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 3, 2017· Cell Distributors

Recalled Item: Tears (Carboxymethylcellulose Sodium Solution) 0.5% Recalled by Cell...

The Issue: Labeling: Not elsewhere classified; product labeling lacks a NDC number, net...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRADIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRONE Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRADIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 3, 2017· Medisca, Inc.

Recalled Item: ESTRIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...

The Issue: cGMP Deviations; manufacturer initiated recall of API product after...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 3, 2017· Mederi Therapeutics, Inc

Recalled Item: Mederi Stretta Catheter and Accessory Kit Recalled by Mederi Therapeutics,...

The Issue: Product sterility compromised due to breach in sterile barrier package

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2017· Natus Medical Incorporated

Recalled Item: Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between...

The Issue: The second generation neoBLUE 2 lights with a black band, sold from 2003 to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2017· Beckman Coulter Inc.

Recalled Item: AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter has confirmed that the Export feature located in the Results...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodApril 1, 2017· Killer Brownie Distributing LLC

Recalled Item: ORIGINAL KB KILLER BROWNIE¿ 3x35 CT NET WT 36 LBS (16.33 kg) CONTAINS: Milk...

The Issue: The firm was notified by a customer that they received product that was...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 1, 2017· Killer Brownie Distributing LLC

Recalled Item: GERMAN CHOCOLATE KB KILLER BROWNIE¿ 3x35 CT NET WT 36 Recalled by Killer...

The Issue: The firm was notified by a customer that they received product that was...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 1, 2017· Killer Brownie Distributing LLC

Recalled Item: PEANUT BUTTER KB KILLER BROWNIE¿ 3x35 CT NET WT 36 lbs (16.33 kg) CONTAINS:...

The Issue: The firm was notified by a customer that they received product that was...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 1, 2017· Killer Brownie Distributing LLC

Recalled Item: NOT-A-NUTTER KB KILLER BROWNIE¿ 3x35 CT NET WT 36 LBS (16.33 kg) CONTAINS:...

The Issue: The firm was notified by a customer that they received product that was...

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 31, 2017· Pinnacle Foods, LLC

Recalled Item: Great Value Bread and Butter Chips 24 Fl Oz. Distributed by: Wal-Mart Stores...

The Issue: Glass fragments were found in Great Value Bread and Butter Chips.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 31, 2017· ConAgra Foods Inc

Recalled Item: Premium Hunt's Chili Kit Recalled by ConAgra Foods Inc Due to Potential...

The Issue: Potential Salmonella contamination of spice packet within chili kits.

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

Class II — Potential Health HazardOngoing
Refund