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. 2,492 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,492 in last 12 months

Showing 1388113900 of 27,655 recalls

Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Sys2.7 Recalled by Zimmer GmbH Due to An investigation identified that...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Osteofresh arthrodesis drill Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Sys 2.7 Recalled by Zimmer GmbH Due to An investigation identified...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: V-TEK" Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Integra LifeSciences Corp.

Recalled Item: MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way Recalled by...

The Issue: The firm has identified a complaint trend regarding breakage of the LimiTorr...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: CBS micro Recalled by Zimmer GmbH Due to An investigation identified that...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: V-TEK" Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2019· Zimmer GmbH

Recalled Item: V-TEK" Recalled by Zimmer GmbH Due to An investigation identified that the...

The Issue: An investigation identified that the products were possibly manufactured...

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

Class II — Potential Health HazardOngoing