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 2506125080 of 52,120 recalls

Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 1000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 2000 mL Product Usage: A Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2018· Baxter Healthcare Corporation

Recalled Item: EXACTAMIX Empty EVA Bags - 500 mL - Product Usage: Recalled by Baxter...

The Issue: Potential ability to leak once used for compounding.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: PROCARE B20 Patient Monitor Recalled by GE Healthcare, LLC Due to Patient...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: B105/125 Patient Monitor. The device is a portable multiparameter unit...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: PROCARE B40 Patient Monitor Recalled by GE Healthcare, LLC Due to Patient...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: B40i Patient Monitor and B40i Patient Monitor V3 The device Recalled by GE...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2018· GE Healthcare, LLC

Recalled Item: B20i Patient Monitor and B20i V2 Patient Monitor. The device Recalled by GE...

The Issue: Patient monitors may restart due to network overload caused by network...

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

Class II — Potential Health HazardOngoing
DrugSeptember 11, 2018· Torrent Pharma Inc.

Recalled Item: Lamotrigine Extended-Release Tablets Recalled by Torrent Pharma Inc. Due to...

The Issue: Failed Dissolution Specifications: Out of Specification for Dissolution test...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 11, 2018· TiSport, Llc

Recalled Item: TiLite X-Short anti-tip tubes Recalled by TiSport, Llc Due to The anti-tip...

The Issue: The anti-tip tubes potentially fail in certain situations and the...

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

Class II — Potential Health HazardOngoing
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Zinc Sulfate 1 mg/mL MDV Injectable Recalled by Pharm D Solutions, LLC Due...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Trimix QM10 Papaverine 30 mg/Phentolamine 4 mg/Atropine 1 mg/PGE 150...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: HCG Lyopholized 1200 IU Injectable Recalled by Pharm D Solutions, LLC Due to...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Trimix Papaverine/Phentolamine/Alprostadil 30 mg/1 mg/20 mcg Powder Pharm D...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Tri-Mix Papaverine/Phentolamine/Alprostadil 150 mg/5 mg/50 mcg a) Injectable...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Sermorelin/GHRP-2 18 mg/6 mg powder Recalled by Pharm D Solutions, LLC Due...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Bi-Mix Injection Recalled by Pharm D Solutions, LLC Due to Lack of Assurance...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Slenderella Compound Injectable Recalled by Pharm D Solutions, LLC Due to...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: Sermorelin/GHRP-2 9 mg/9 mg Powder Recalled by Pharm D Solutions, LLC Due to...

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
DrugSeptember 10, 2018· Pharm D Solutions, LLC

Recalled Item: HCG Lyophilized 5000 IU Injectable Pharm D Solutions Recalled by Pharm D...

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