Catalog Number 00392501100 |
Device Problem
Failure to Cut (2587)
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Patient Problem
No Patient Involvement (2645)
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Event Date 04/26/2019 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).Foreign - (b)(6).Customer has indicated that the product is in process of being returned to zimmer biomet for investigation.Once the investigation has been completed, a follow-up mdr will be submitted.
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Event Description
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During the kit inspection at zimmer biomet it has been detected that the cable cutter does not cut the cable.This causes the cable to fray or to be crushed.There was no patient involvement.
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Manufacturer Narrative
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The products were evaluated and noted to be operating without any issues.The root cause is determined to be no failure detected - device operated within specifications.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.
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Event Description
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No further event information available at the time of this report.
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Search Alerts/Recalls
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