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. 2,489 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,489 in last 12 months

Showing 2472124740 of 52,120 recalls

DrugOctober 19, 2018· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's 24 Hour Allergy (cetirizine hydrochloride) Oral Solution 1 mg/mL...

The Issue: Failed Impurities/Degradation Specifications: unknown impurity higher than...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2018· Teva Pharmaceuticals USA

Recalled Item: Metoprolol Succinate Extended Release Tablets Recalled by Teva...

The Issue: Failed dissolution specifications: Out-of-Specification dissolution test...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: Fentanyl (10 mcg/mL) in NS 1 mL (in 3mL BD Syringe) Recalled by Avella 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
DrugOctober 19, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: Morphine (1 mg/mL) in NS 100 mL Bag Recalled by Avella of Deer Valley, Inc....

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
DrugOctober 19, 2018· Avella of Deer Valley, Inc. Store 38

Recalled Item: Phenylephrine 30 mg added to NS 250 mL Bag Recalled by Avella of Deer...

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
FoodOctober 19, 2018· U.B.C. Food Distributors INC.

Recalled Item: Baraka Mild Curry Powder packed in 7 oz. Plastic Jar Recalled by U.B.C. Food...

The Issue: UBC FOOD Distributors initiated a voluntary recall of Baraka Hot and Mild...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 19, 2018· Karlsburger Foods, Inc.

Recalled Item: Karlsburger Kitchens Roasted Onion Base Recalled by Karlsburger Foods, Inc....

The Issue: Firm is recalling a Roasted Onion Base product due to potential Listeria...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 19, 2018· U.B.C. Food Distributors INC.

Recalled Item: Baraka Hot Curry Powder packed in 7 OZ Plastic Jar Recalled by U.B.C. Food...

The Issue: UBC FOOD Distributors initiated a voluntary recall of Baraka Hot and Mild...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 19, 2018· Simply Fresh Foods, Inc

Recalled Item: Rojo's Autentico Black Bean 5 Layer Dip Recalled by Simply Fresh Foods, Inc...

The Issue: Firm was notified by McCain Foods that the corn used in their layer dip is...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 18, 2018· Trident Seafoods Corporation

Recalled Item: Kroger brand. Frozen non-ready to eat Alaskan Salmon Bites Recalled by...

The Issue: Frozen non-ready to eat Alaskan Salmon Bites, Kroger brand, are recalled due...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 40 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Slice (Air) Recalled by Philips Medical Systems (Cleveland)...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· EUROTROL INC

Recalled Item: HemoTrol Level 3- In Vitro Diagnostic Hematology quality control mixture....

The Issue: Incorrect measurement results caused by microbial contamination of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 16 Slice (Power) Recalled by Philips Medical Systems (Cleveland)...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 10 Slice (Air) Recalled by Philips Medical Systems (Cleveland)...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· EUROTROL INC

Recalled Item: HemoTrol Level 2- In Vitro Diagnostic Hematology quality control mixture...

The Issue: Incorrect measurement results caused by microbial contamination of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 6 Slice (Air) Recalled by Philips Medical Systems (Cleveland) Inc...

The Issue: There is a potential for separation of fiberglass resin which may cause the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2018· Beckman Coulter Inc.

Recalled Item: iChem VELOCITY Urine Chemistry Strips Recalled by Beckman Coulter Inc. Due...

The Issue: Falsely elevated (false positive) urobilinogen patient results due to an...

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

Class II — Potential Health HazardOngoing
DrugOctober 18, 2018· H J Harkins Company Inc dba Pharma Pac

Recalled Item: GENTAMICIN OPTH-SOL 5ml Compare: Garamycin. 5-mL plastic dropper bottle...

The Issue: Presence of Particulate Matter: Crystalline particles were noticed by...

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

Class II — Potential Health HazardOngoing
Refund