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 2608126100 of 29,186 recalls

Medical DeviceSeptember 18, 2013· Richard Wolf Medical Instruments Corp.

Recalled Item: Individual units labeled in part: Recalled by Richard Wolf Medical...

The Issue: Richard Wolf Medical Instrument Corporation recieved a complaint stating...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension LOCI TNI Troponin I Calibrator RC 621. The Recalled by...

The Issue: Siemens Dimension LOCI TNI Troponin I calibrator lot 3DD007 may demonstrate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: DeRoyal (R) Aquarius Hot/Cold Therapy Combo Unit Recalled by DeRoyal...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2013· DeRoyal Industries Inc

Recalled Item: Aquarius (TM) TEMPERATURE THERAPY Recalled by DeRoyal Industries Inc Due to...

The Issue: The unit displays an error code of hose kinking when no hose kink is...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Carestream Health Inc.

Recalled Item: Carestream Vue PACS Recalled by Carestream Health Inc. Due to Carestream...

The Issue: Carestream Health, Inc. has issued a recall when using the CARESTREAM Client...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences EMBOL-X Glide Protection System Recalled by Edwards...

The Issue: Edwards Lifesciences is recalling certain lots of EMBOL-X Glide Protection...

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

Class I — Serious Health HazardOngoing