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. 2,478 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,478 in last 12 months

Showing 2832128340 of 52,120 recalls

Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: PROPONENT EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE MRI DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE MRI SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ALTRUA 2 SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO MRI SR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO MRI EL DR Pacemaker Recalled by Boston Scientific Corporation Due...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ACCOLADE EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: VALITUDE X4 CRT-P Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO EL DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: VISIONIST X4 CRT-P Pacemaker Recalled by Boston Scientific Corporation Due...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: PROPONENT VDD SL Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ALTRUA 2 DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: ESSENTIO MRI DR Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 7, 2017· Boston Scientific Corporation

Recalled Item: PROPONENT MRI Pacemaker Recalled by Boston Scientific Corporation Due to...

The Issue: Boston Scientific has received reports of intermittent over-sensing of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2017· Intel-GE Care Innovations LLC

Recalled Item: Health Harmony Mobile application software Product Usage: Care Innovations...

The Issue: It was discovered that in certain situations, including partial sessions and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2017· Reliance Medical Products Inc

Recalled Item: Suspension Arm (P/N: 525004 Recalled by Reliance Medical Products Inc Due to...

The Issue: Product has been found with a missing Washer, Retaining Ring, and/or Stop...

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

Class II — Potential Health HazardOngoing
DrugDecember 5, 2017· Sanofi-Aventis U.S. LLC

Recalled Item: Enoxaparin Sodium Recalled by Sanofi-Aventis U.S. LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength. A single syringe labeled as 150...

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

Class III — Low RiskOngoing
Refund
FoodDecember 5, 2017· Creative Contract Packaging Corporation, LLC

Recalled Item: HERB-OX Beef Flavor Granulated Bouillon Recalled by Creative Contract...

The Issue: Creative Contract Packaging LLC is voluntarily recalling two code dates of...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2017· AuroMedics Pharma LLC

Recalled Item: Pantoprazole Sodium for Injection Recalled by AuroMedics Pharma LLC Due to...

The Issue: Presence of Particulate Matter: One vial from a lot of Pantoprazole Sodium...

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

Class I — Serious Health HazardOngoing
Refund