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. 2,452 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,452 in last 12 months

Showing 3638136400 of 52,120 recalls

DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Genzyme Corporation

Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...

The Issue: Presence of Particulate Matter: Glass particles found in the product after...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 16, 2016· Actavis Elizabeth LLC

Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 15, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...

The Issue: Siemens is initiating this recall due to a potential malfunction and hence...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Ivoclar Vivadent, Inc.

Recalled Item: Helioseal Clear 1 x 1.25 g Recalled by Ivoclar Vivadent, Inc. Due to...

The Issue: Complaints were received claiming the material failed to polymerize under...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Inspiration with Tomosynthesis functionality Recalled by Siemens...

The Issue: A potential system fatal error may occur during tomosynthesis reconstruction...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· CareFusion 303, Inc.

Recalled Item: Alaris PC Unit Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the Alaris PC unit because a component on the PC...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Zimmer Spine, Inc.

Recalled Item: Universal Clamp¿ System (IFU : SNA027-N-90001). Provides the stability...

The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Zimmer Spine, Inc.

Recalled Item: Instinct¿ Java¿ System (IFU : 046WAN0000T) . Stabilizes one or Recalled by...

The Issue: Zimmer Biomet is initiating a Medical Device Correction Notice to provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Biomet Spine, LLC

Recalled Item: 10mm X 12o Solitaire Ti Medium Spacer  Solitaire Anterior Spinal System...

The Issue: Zimmer Biomet Spine initiated a recall of certain Solitaire Ti Spacers...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2016· Becton Dickinson & Co.

Recalled Item: BD SurePathTM Preservative Collection Vials Recalled by Becton Dickinson &...

The Issue: BD has confirmed that a portion of BD SurePath" collection vials associated...

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

Class II — Potential Health HazardOngoing