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OmniGuide Recalls

1 recall on record · December 12, 2012 to December 12, 2012 · Medical Devices

December 12, 2012Medical DevicesFDA

OmniGuide, Inc. recalls OmniGuide BP-ROBOTIC ( BeamPath Robotic), Single Use Cat. # BP-ROBOTIC The OmniGuide Fiber is indicated for the inci

Hazard: Failure of glue joint, allowed a portion of the single use device to shift inside, may separate and fall into the patient

OmniGuide Recalls | RecallWatchUSA