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. 1,849 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
1,849 in last 12 months

Showing 3162131640 of 52,120 recalls

Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: PRK Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Vitrectomy Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Ophthalmic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Dr. Wischmeier Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Vitrectomy Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Setup Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Lasik Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: ENT Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Cataract Kit - Dr. Slingsby Recalled by Windstone Medical Packaging, Inc....

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Minor Operation Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Cataract Kit Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Eye Cataract Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Custom Tray Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Eye Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2017· Windstone Medical Packaging, Inc.

Recalled Item: Plastic Pack Recalled by Windstone Medical Packaging, Inc. Due to AMS custom...

The Issue: AMS custom kits containing Medtronic Covidien Curity Eye Pad are recalled...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER Recalled by Intuitive Surgical, Inc. Due to Intuitive Surgical has...

The Issue: Intuitive Surgical has become aware and further investigation has determined...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 12MM Product Number: Recalled...

The Issue: Potential for the cutting blade to detach from the device and/or the distal...

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

Class II — Potential Health HazardOngoing