Product Recalls in Maine

Product recalls affecting Maine — including food, drugs, consumer products, medical devices, and vehicles distributed to Maine. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,404 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,404 in last 12 months

Showing 1800118020 of 27,655 recalls

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: 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: 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: Ortho Basic 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: 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 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: 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: 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: 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: 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 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· 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· 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· 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· 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· 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· 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· 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