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. 1,849 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
1,849 in last 12 months

Showing 3150131520 of 52,120 recalls

DrugMarch 28, 2017· Teva Pharmaceuticals USA

Recalled Item: PrednisoLONE Oral Solution USP Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Stability Specifications

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

Class III — Low RiskOngoing
Refund
DrugMarch 28, 2017· Envy Me

Recalled Item: LaBri's Body Health Atomic Recalled by Envy Me Due to Undeclared Sibutramine

The Issue: Marketed without an approved NDA/ANDA: Product contains undeclared Sibutramine.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 27, 2017· Alcon Research, Ltd.

Recalled Item: Alcon Patient Care Kits Product Usage: A Patient Care Kit Recalled by Alcon...

The Issue: Alcon is initiating a Voluntary Medical Device Removal because the product...

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

Class II — Potential Health HazardOngoing
FoodMarch 27, 2017· The French's Food Company, LLC SUBS Reckitt Benckiser

Recalled Item: French's Crispy Jalapenos Net Wt. 5 oz. (141.7g) Recalled by The French's...

The Issue: Product may contain foreign objects: rocks and metal fragments.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex Bio Composite SwiveLock SP Vented Recalled by Arthrex, Inc. Due to...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex Bio-SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Dale Medical Products, Inc.

Recalled Item: Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Recalled...

The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Remel Inc

Recalled Item: Blood Agar (TSA w/ 5% Sheep Blood) Plate Recalled by Remel Inc Due to...

The Issue: Confirmed complaint of surface contamination of Listeria monocytogenes.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Dale Medical Products, Inc.

Recalled Item: Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Recalled...

The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estradiol Non-Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co....

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Testosterone Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co....

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estradiol Micronized Bulk Recalled by Qinhuangdao Zizhu Pharmaceutical, Co....

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estrone Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co. Due to...

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Ethinyl Estradiol Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical,...

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Levonorgestrel Non-Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical,...

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estriol Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co. Due to...

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund