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 2674126760 of 27,655 recalls

Medical DeviceAugust 2, 2012· Hospira, Inc.

Recalled Item: Sterile Empty Vial and Injector (30mL PCA vial) Recalled by Hospira, Inc....

The Issue: Reports of leaking during filling and administration.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2012· Steris Corporation

Recalled Item: 100 ft roll of tubing inside a cardboard box. Medical Recalled by Steris...

The Issue: On 7/20/2012 the firm became aware that a lot of tubing was distributed by...

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

Class III — Low RiskOngoing
Medical DeviceAugust 1, 2012· Nellcor Puritan Bennett Inc. (dba Covidien LP)

Recalled Item: DGPHP RFA High-Power Single Use Grounding Pads and Cool-Tip RFA Recalled by...

The Issue: Covidien is conducting a recall of various production lots of DGHP RFA High...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· Steris Corporation

Recalled Item: The SYSTEM 1E Liquid Sterilant Processing System. The SYSTEM 1E Recalled by...

The Issue: The firm initiated a recall after complaint investigations revealed that...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx 15kw Mobile X-Ray System The Recalled by GE...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 200 amx with Digital Upgrade. The Recalled by GE...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2012· GE Healthcare, LLC

Recalled Item: GE Healthcare Optima XR 220amx 30kw Mobile X-ray System The Recalled by GE...

The Issue: GE Healthcare has become aware of a software issue on the interface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2012· DePuy Orthopaedics, Inc.

Recalled Item: DePuy Custom Implant Devices Packaging: Packaging was not standardized on...

The Issue: In connection with a Warning Letter received from the U.S. Food & Drug...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 31, 2012· Respironics California Inc

Recalled Item: V60 Ventilator Recalled by Respironics California Inc Due to Respironics is...

The Issue: Respironics is recalling the V60 ventilator because certain blower motor...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 30, 2012· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Emit(R) 2000 Phenobarbital Assay (OSR4D229) and Syva(R) Emit(R)...

The Issue: Firm has confirmed highter imprecision with the recalled lots on Beckman...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2012· AGFA Corp.

Recalled Item: IMPAX Cardiovascular (CV) Reporting Reporting tool used for structured...

The Issue: Content entered into the "Conclusions" free text box on the Report Writer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2012· Quality Electrodynamics LLC

Recalled Item: TxRx Knee 15 Coil 3T. For use in conjunction with Recalled by Quality...

The Issue: On July 27, 2012, it was reported to the firm that the Siemens 3T 15ch Knee...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2012· Integra Limited

Recalled Item: The MAYFIELD¿ Horseshoe Gel Pads are used in conjunction with Recalled by...

The Issue: An investigation of customer complaints identified that for two product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2012· Bio-Rad Laboratories

Recalled Item: The Bio-Rad MONOLISA Anti-HBs EIA is for In Vitro Diagnostic Recalled by...

The Issue: Prolonged exposure of the MONOLISA Anti-HBs EIA Conjugate Diluent component...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2012· Elekta, Inc.

Recalled Item: Multileaf Collimator To be used for single or multiple fractions Recalled by...

The Issue: Information released with the product Agility did not originally contain...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 27, 2012· Integra Limited

Recalled Item: The MAYFIELD¿ Horseshoe Gel Pads are used in conjunction with Recalled by...

The Issue: An investigation of customer complaints identified that for two product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Serial interface module RS-232 Product Usage: The System 1 provides Recalled...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Serial interface module RS-485 Product Usage: The System 1 provides Recalled...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Interface module for CDl System 500 Product Usage: The Interface Recalled by...

The Issue: Terumo Cardiovascular Systems has received reports of malfunctions involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 26, 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 sent a Safety Advisory (AA-2010-007-C) on...

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

Class II — Potential Health HazardOngoing