Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,549 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,549 in last 12 months

Showing 5130151320 of 53,623 recalls

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· 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 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· Maquet Inc.

Recalled Item: Maquet Yuno Extension Table Device Maquet GmbH & Co. KG Recalled by Maquet...

The Issue: There is a potential issue with the screw tension of the extension device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2012· Brookstone Company, Inc.

Recalled Item: Brookstone Heated Body Bean Recalled by Brookstone Company, Inc. Due to...

The Issue: Additional Warning Statement to prevent burns to the skin

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· 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
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 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 1, 2012· Merge Healthcare, Inc.

Recalled Item: CADstream software. Product Usage: CADstream is an image processing system...

The Issue: An incorrect biopsy or missed target could result if the incorrect grid is...

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

Class II — Potential Health HazardOngoing