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. 2,475 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,475 in last 12 months

Showing 3150131520 of 52,120 recalls

Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Delta XL Recalled by Draegar Medical Systems, Inc. Due to It was reported...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Kappa Recalled by Draegar Medical Systems, Inc. Due to It was reported that...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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 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
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
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: 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: 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
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Craftmatic Model 1 Base for Dual Bed Configurations Recalled by Craftmatic...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

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

Recalled Item: Legacy Base for Dual Bed Configurations Recalled by Craftmatic Industries,...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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· 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
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 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 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