🔔 Product Recalls & Refunds in Minnesota

8 active product recalls & refunds in minnesota — verified and updated daily.

Product Recalls & Refunds in Minnesota (8 active)

J and J Bunting, Inc: Lunds & Byerly's Curry Powder Sweet FDA food recall — return recalled product to store for a full refund of purchase price

Recall reason: Sesame Seeds White were labeled as Curry Powder Sweet.. Recalled by J and J Bunting, Inc. Distribution: WI. Classification (Class II — potential

Product Recall MN

Smiths Medical ASD Inc.: paraPAC 300 ventilator kit without internal PEEP and CPAP, Item Number P300N FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Smiths Medical became aware of an issue related to a potential for the patient outlet connector to loosen/detach from the paraPAC Plus P300 and P…

Product Recall MN

Boston Scientific Corporation: EMBLEM MRI S-ICD Pulse Generator Model A219; Subcutaneous Implantable Cardioverter Defibrillator FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: There is a potential for a rare interaction between the EMBLEM S-ICD and LATITUDE communicator, which may cause S-ICD sensing disablement for a 2…

Product Recall MN

Smiths Medical ASD Inc.: paraPAC plus 310 ventilator kit with internal PEEP and CPAP, Item Number P310N FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Smiths Medical became aware of an issue related to a potential for the patient outlet connector to loosen/detach from the paraPAC Plus P300 and P…

Product Recall MN

Smiths Medical ASD Inc.: Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NXX FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: There is a potential for inadvertent tidal volume knob movement from the original setting when set at high (1000-1500 mL) and low (70-150 mL) set…

Product Recall MN

Boston Scientific Corporation: EMBLEM S-ICD Pulse Generator Model A209; Subcutaneous Implantable Cardioverter Defibrillator FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: There is a potential for a rare interaction between the EMBLEM S-ICD and LATITUDE communicator, which may cause S-ICD sensing disablement for a 2…

Product Recall MN

IntegraDose Compounding Services LLC: Vasopressin 2 Unit/2 mL in 0.9% Sodium Chloride, 2 mL per syringe, Rx Only, 719 Kasota Ave SE, Minneapolis, MN. NDC 71139-0190-1 FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Subpotent Drug. Recalled by IntegraDose Compounding Services LLC. Distribution: MN only. Classification (Class II — potential health risk). Affe…

Product Recall MN

IntegraDose Compounding Services LLC: Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile Syringe for Injection, Concentration: 1 Unit/mL, 2 mL Syringe, Rx Only, 719 Kasota Ave SE, Minneapolis, MN, Compounded Drug Not for Resale. Office Use Only FDA drug recall — return recalled medication to your pharmacy for a full refund of purchase price

Recall reason: Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.. Recalled by IntegraDose Compounding…

Product Recall MN

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