The catalog number and lot code were not provided.The device was reported as an unknown 10 degree 36 e liner.The other device noted in this report is an unknown ceramic head.It cannot be determined which, if either of these devices may have caused or contributed to the patient's experience.It was noted that the device is not available for evaluation due to hospital policy.Additional information has been requested and if received, will be provided in the supplemental report upon completion of the investigation.
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