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. 1,015 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
1,015 in last 12 months

Showing 31861–31880 of 52,120 recalls

FoodMarch 3, 2017· The SoyNut Butter Company

Recalled Item: Dixie Diners' Club Carb Not Beanit Butter Recalled by The SoyNut Butter...

The Issue: Potential contamination of product with E. coli O157.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· The SoyNut Butter Company

Recalled Item: I.M. Healthy Apple Granola Recalled by The SoyNut Butter Company Due to...

The Issue: Potential contamination of product with E. coli O157.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· Vulto Creamery

Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· The SoyNut Butter Company

Recalled Item: I.M. Healthy Recalled by The SoyNut Butter Company Due to Potential E. coli...

The Issue: Potential contamination of product with E. coli O157.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· The SoyNut Butter Company

Recalled Item: I.M. Healthy Recalled by The SoyNut Butter Company Due to Potential E. coli...

The Issue: Potential contamination of product with E. coli O157.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· The SoyNut Butter Company

Recalled Item: I.M. Healthy Recalled by The SoyNut Butter Company Due to Potential E. coli...

The Issue: Potential contamination of product with E. coli O157.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· Vulto Creamery

Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· Vulto Creamery

Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· Vulto Creamery

Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· Vulto Creamery

Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 2, 2017· Philips Visicu

Recalled Item: eCare Coordinator Product Usage: is software intended for use in Recalled by...

The Issue: eCareCoordinator (eCC) is intended for use in data aggregation, patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2017· Myelotec, Inc.

Recalled Item: Myelotec Video Guided Catheters Recalled by Myelotec, Inc. Due to...

The Issue: Obstructed/blocked port from defective VGC Access Port Body component.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2017· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...

The Issue: Ortho Kinematics notified customers that errors were contained in...

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

Class II — Potential Health HazardOngoing
DrugMarch 2, 2017· Fougera Pharmaceuticals Inc.

Recalled Item: Desonide Ointment Recalled by Fougera Pharmaceuticals Inc. Due to Labeling:...

The Issue: Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 1, 2017· Signature Club A Ltd

Recalled Item: Double Hyaluronic 1000 Recalled by Signature Club A Ltd Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: odor complaint of product...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2017· G & W Laboratories, Inc.

Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by G & W Laboratories,...

The Issue: CGMP Deviations: an expired active ingredient was used in the manufacture of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental malefemale taper Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 14mmdx50cm left Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 16mmdx38cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing