Model Number N/A |
Device Problem
Failure to Cut (2587)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 09/11/2020 |
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 an evaluation of this device is completed, a follow-up/final report will be submitted.Telephone number: (b)(6).
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Event Description
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During surgery when blade was inserted and pressure applied to the skin of the patient, the hand piece did not cut/graft the skin.No adverse events were reported as a result of this malfunction.
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Event Description
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No new event information.
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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 motor speed was not stable and had signs of oxidation.The motor was replaced and resolved the reported issue.Review of the device history record identified no deviations or anomalies during manufacturing related to the reported event.Device is used for treatment.Review of complaint history identified additional similar complaints for the reported item and part and lot combination.Complaints are monitored through monthly complaint review in order to identify potential adverse trends.A definitive root cause cannot be determined.No corrective actions, preventive actions, or field actions resulted after investigation of this event.The event is confirmed.
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Search Alerts/Recalls
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