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. 2,693 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,693 in last 12 months

Showing 28812900 of 52,120 recalls

DrugMarch 7, 2025· Slate Run Pharmaceuticals

Recalled Item: Cinacalcet Hydrochloride Tablets 60 mg Recalled by Slate Run Pharmaceuticals...

The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Mylan Institutional, Inc.

Recalled Item: Levothyroxine Sodium Tablets Recalled by Mylan Institutional, Inc. Due to...

The Issue: Super-Potent Drug: Out of specification potency results were obtained.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 7, 2025· Slate Run Pharmaceuticals

Recalled Item: Cinacalcet Hydrochloride Tablets 30 mg Recalled by Slate Run Pharmaceuticals...

The Issue: CGMP deviations: The presence of nitrosamine impurity above the acceptable...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH Recalled by Ethicon Endo...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2025· Ethicon Endo Surgery, LLC

Recalled Item: PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1 Recalled by Ethicon Endo Surgery,...

The Issue: Identified curing issues with the silicone during the needles manufacturing...

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

Class II — Potential Health HazardOngoing
DrugMarch 6, 2025· QuVa Pharma, Inc.

Recalled Item: fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.125% Bupivacaine Recalled...

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
DrugMarch 6, 2025· QuVa Pharma, Inc.

Recalled Item: fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.1% Bupivacaine 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
DrugMarch 6, 2025· QuVa Pharma, Inc.

Recalled Item: fentaNYL Citrate PF 200 mcg/100 mL (2 mcg/ml) /0.2% ROPivacaine 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
Medical DeviceMarch 6, 2025· GE Medical Systems, LLC

Recalled Item: Venue Go Models: R2 (Model Number H45181VG) Recalled by GE Medical Systems,...

The Issue: The battery for certain ultrasound systems can potentially develop an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2025· GE Medical Systems, LLC

Recalled Item: Venue Fit Models: R3 (Model Number H45303VFSC Recalled by GE Medical...

The Issue: The battery for certain ultrasound systems can potentially develop an...

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

Class II — Potential Health HazardOngoing
DrugMarch 5, 2025· L'Oreal USA

Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne...

The Issue: cGMP Deviations: The recall was initiated due to detected trace levels of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· L'Oreal USA

Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne...

The Issue: cGMP Deviations: The recall was initiated due to detected trace levels of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· L'Oreal USA

Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne...

The Issue: Chemical Contamination: This recall has been initiated due to detected trace...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· Golden State Medical Supply Inc.

Recalled Item: PRASUGREL TABLETS Recalled by Golden State Medical Supply Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· Strides Pharma, Inc.

Recalled Item: Testosterone Gel 1% Recalled by Strides Pharma, Inc. Due to Presence of...

The Issue: Presence of foreign substance: Presence of Benzene.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· Strides Pharma, Inc.

Recalled Item: Testosterone Gel 1% Recalled by Strides Pharma, Inc. Due to Presence of...

The Issue: Presence of foreign substance: Presence of Benzene.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Rising Pharma Holding, Inc....

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Coracoid Clamp Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing