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. 2,519 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,519 in last 12 months

Showing 1926119280 of 29,186 recalls

Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Universal Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Facial Plastic Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Lap Gallbladder Pack Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Lower Extremity Pack Recalled by Windstone Medical Packaging, Inc. Due to...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Bayview Abdominoplasty Pack Recalled by Windstone Medical Packaging, Inc....

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Breast Recon Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Hernia Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Stem Pack Recalled by Windstone Medical Packaging, Inc. Due to The Medtronic...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Breast Augmentation Pack Recalled by Windstone Medical Packaging, Inc. Due...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Open Procedure Pack Recalled by Windstone Medical Packaging, Inc. Due to The...

The Issue: The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Arrow International Inc

Recalled Item: Vascular catheter introduction kit The PICC is indicated for short Recalled...

The Issue: There have been complaints for peel away sheaths flaring

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Siemens Healthcare Diagnostics, Inc.

Recalled Item: N Latex HCY REAGENT Recalled by Siemens Healthcare Diagnostics, Inc. Due to...

The Issue: The firm confirmed a reduced once-opened and on-board stability for N Latex...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Mammomat Inspiration full Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Software error

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Kiscomedica S.A.

Recalled Item: L-Varlock Cage/Trial Implant Holder Recalled by Kiscomedica S.A. Due to Firm...

The Issue: Firm received a complaint of the tip holder breaking during use.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2017· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Version 2.3.252. VMA software is a Recalled...

The Issue: Ortho Kinematics Inc. sent a Notice of Correction to Released Testing...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Elekta, Inc.

Recalled Item: Monaco RTP System. Used to make treatment plans for patients Recalled by...

The Issue: Incorrect dose after editing beam number an wedge angle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Encore Medical, Lp

Recalled Item: Empowr PS Knee Tibial Insert Recalled by Encore Medical, Lp Due to The...

The Issue: The Empowr PS Insert was reported as missing the impaction slot feature.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2017· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens ADVIA Centaur Systems Calibrator A Kits Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics has confirmed a negative bias for ADVIA...

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

Class II — Potential Health HazardOngoing