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 2634126360 of 27,655 recalls

Medical DeviceNovember 5, 2012· OmniGuide, Inc.

Recalled Item: OmniGuide BP-ROBOTIC ( BeamPath Robotic) Recalled by OmniGuide, Inc. Due to...

The Issue: Failure of glue joint, allowed a portion of the single use device to shift...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2012· Applied Medical Resources Corp

Recalled Item: Laparoscope Recalled by Applied Medical Resources Corp Due to Applied...

The Issue: Applied Medical is conducting a voluntary recall on a specific lot number of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2012· Integra LifeSciences Corporation

Recalled Item: MAYFIELD Composite Series Base Unit Recalled by Integra LifeSciences...

The Issue: An investigation of an adverse trend of complaints conducted by Integra...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2012· Beckman Coulter Inc.

Recalled Item: The Access hLH assay is a paramagnetic particle Recalled by Beckman Coulter...

The Issue: Beckman Coulter Inc. (BEC) has demonstrated that real time stability testing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2012· Integra LifeSciences Corporation

Recalled Item: MAYFIELD Composite Series Skull Clamps Recalled by Integra LifeSciences...

The Issue: An investigation of an adverse trend of complaints conducted by Integra...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2012· Arobella Medical, LLC

Recalled Item: Arobella Medical 6mm Qurette used with the Arobella Medical AR1000 Recalled...

The Issue: This recall has been initiated because the Arobella Medical 6mm Qurette Q07...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2012· Medrad Inc

Recalled Item: MEDRAD Hand Controller Sheath Recalled by Medrad Inc Due to The seal between...

The Issue: The seal between the white polyethylene and the clear plastic may be missing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 5, 2012· Ansell Healthcare Products LLC

Recalled Item: Lifestyles Pleasure Collection 30 Premium Lubricated Condoms Assortment of...

The Issue: One lot of Lifestyles Pleasure Collection Lubricated Condoms is misbranded....

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Standard ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· Del Mar Reynolds Medical, Ltd.

Recalled Item: BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators are...

The Issue: The BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators were...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· Synthes USA HQ, Inc.

Recalled Item: Synthes Trauma Nail System. The devices are indication for bone fixation....

The Issue: Recall was initiated due to the possibility that the outer pouch was...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD Flexible ClearSeal SINGLE USE Recalled by King Systems Corp. Due to...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· King Systems Corp.

Recalled Item: KING LAD SILI CONE SINGLE USE Recalled by King Systems Corp. Due to The firm...

The Issue: The firm received two complaints from a user facility in New Jersey...

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

Class II — Potential Health HazardOngoing