A device was returned to a third-party service center in reference to the voluntary field safety notice / recall notification related to the sound abatement foam in certain cpap, bipap, and mechanical ventilator devices.During the evaluation of the device, the third-party service center visually inspected the device and found no evidence of foam degradation found in the assembly.Error code: 193 was noted.In addition to the above findings, there was a secondary finding of calcium particles.The device was scrapped.
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