Model Number N/A |
Device Problem
Failure to Cut (2587)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 11/26/2021 |
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 was reported that during testing the device did not cut properly.There was no reported adverse event as it relates to this event.
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Manufacturer Narrative
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This complaint has been recorded under (b)(4).Review of the most recent repair record determined head and control bar were worn and replaced and resolved the reported issue.Device is used for treatment.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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Event Description
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No additional information is available.
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Search Alerts/Recalls
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