Model Number N/A |
Device Problems
Failure to Cut (2587); Output Problem (3005)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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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 (b)(4).Once the investigation 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, date unknown.No adverse event was 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 determined that the control bar was out of position.The control bar was reposition and resolved the reported issue.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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