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Model Number 0940023000 |
Device Problem
Fracture (1260)
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Patient Problem
No Patient Involvement (2645)
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Event Date 10/16/2019 |
Event Type
malfunction
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Manufacturer Narrative
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A follow up report will be filed once the quality investigation is complete.Awaiting return of device to manufacturer.
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Event Description
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It was reported via the customer that, they observed a broken blade within their inventory.It was also reported that this event did not occur during a surgical procedure, and there was no patient involvement, no delay and no adverse consequences as a result of this event.
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Manufacturer Narrative
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The reported event, for blade breakage, was not confirmed as the blade was not returned for evaluation.Without the blade, the root cause cannot be determined.Device not available for return.
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Event Description
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It was reported via the customer that, they observed a broken blade within their inventory.It was also reported that this event did not occur during a surgical procedure, and there was no patient involvement, no delay and no adverse consequences as a result of this event.
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Search Alerts/Recalls
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