Model Number N/A |
Device Problem
Intermittent Loss of Power (4016)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 09/18/2020 |
Event Type
malfunction
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Manufacturer Narrative
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This event has been recorded by zimmer biomet under cmp(b)(4).Once an evaluation of this device is completed, a follow-up/final report will be submitted.
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Event Description
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It was reported that the device stopped working during surgery and that there was no procedure delay nor harm/injury to any person involved.No adverse events have been reported as a result of this malfunction.
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Manufacturer Narrative
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This event has been recorded by zimmer biomet under (b)(4).This medwatch is being filed to relay additional information.Review of the most recent repair record could not be completed because the device was not returned for evaluation and repair.Review of the device history record identified no deviations or anomalies during manufacturing.Device is used for treatment.A definitive root cause cannot be determined.The event cannot be confirmed.
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Event Description
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There is no additional information.
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Search Alerts/Recalls
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