Model Number N/A |
Device Problems
Incorrect Measurement (1383); Failure to Cut (2587)
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Patient Problem
Insufficient Information (4580)
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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 has been reported that the dermatome was cutting too deep during a procedure.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).Review of the most recent repair record identified no repairs related to the reported event.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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