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. 2,355 recalls have been distributed to Maine in the last 12 months.

48,770 total recalls
2,355 in last 12 months

Showing 2690126920 of 27,655 recalls

Medical DeviceJune 26, 2012· GE Healthcare, LLC

Recalled Item: GE Giraffe and Panda T-Piece Resuscitation System labeled ***T-Piece...

The Issue: Disposable T-Piece circuits used with resuscitation systems are unable to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 26, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...

The Issue: GE Healthcare has recently become aware of a potential issue due to an...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V. The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 25, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) has received reports of various...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Central Control Module for System 1: System 1 Base Recalled by Terumo...

The Issue: Terumo CVS has received reports of the Central Control Monitor (CCM) for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Central Control Module for System 1: System 1 Base Recalled by Terumo...

The Issue: Terumo CVS has received reports of the Central Control Monitor (CCM) for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Advanced Perfusion System 1 battery charge is being depleted faster...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 220/240V The Terumo¿ Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received eight complaints since...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo Advanced Perfusion System 1 battery charge is being depleted faster...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base 100/120V The Terumo¿ Advanced Perfusion System 1 Recalled by...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received eight complaints since...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Electronic O2 Blender/Analyzer. The...

The Issue: Terumo Cardiovascular Systems (Terumo CVS) received two complaints related...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo¿ Advanced Perfusion System 1 has displayed a Red X error message on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Elekta, Inc.

Recalled Item: Focal SIM Planning of radiation therapy Recalled by Elekta, Inc. Due to...

The Issue: Incorrect patient shift directions when the Setup dialog is printed out when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Elekta, Inc.

Recalled Item: Monaco Product Usage: Planning of radiation therapy Recalled by Elekta, Inc....

The Issue: Incorrect patient shift directions when the Setup dialog is printed out when...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: System 1 Base Recalled by Terumo Cardiovascular Systems Corporation Due to...

The Issue: Terumo¿ Advanced Perfusion System 1 has displayed a Red X error message on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 System 1 Base Recalled by Terumo...

The Issue: Terumo Cardiovascular Systems has received reports of several issues that...

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

Class II — Potential Health HazardOngoing