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Catalog Number 05.001.204 |
Device Problems
Bent (1059); Charging Problem (2892)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Type
malfunction
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Manufacturer Narrative
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Initial reporter's phone number: (b)(6).The actual device has been returned and is currently pending evaluation.Once reliability engineering evaluates the device, a supplemental medwatch report will be sent accordingly.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
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Event Description
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It was reported by (b)(4) that during service and evaluation, it was observed that the universal battery charger device had a charging bay defect as the red led was illuminated.It was noted in the service order that the 1 and 3 charging sockets were defective and bent; and "update (dissolved label usb)." this event did not occur during surgery.There was no patient involvement.There were no reports of injuries, medical intervention or prolonged hospitalization.The exact date of this event was unknown.All available information has been disclosed.If additional information should become available, a supplemental medwatch report will be submitted accordingly.
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Manufacturer Narrative
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This device was returned for service; however, did not meet manufacturing specifications during pre-repair assessment.Reliability engineering evaluated the device and observed red led was illuminated and the charging bay was defective.Therefore, the reported condition was confirmed.It was further determined that 1 and 3 charging sockets were defective, updated usb label was dissolved, and the device was bent.The assignable root cause was determined to be due to improper/faulty handling.This was further defined as user error/misuse/abuse.If additional information should become available, a supplemental medwatch report will be sent accordingly.
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Search Alerts/Recalls
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