Model Number N/A |
Device Problems
Deflation Problem (1149); Gas/Air Leak (2946)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Type
malfunction
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Event Description
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It was reported that during pre-op testing, the device was leaking air.No adverse event is associated with this incident.Due diligence is in progress with no response as of yet.If additional information becomes available, a supplemental report will be completed and submitted.
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Manufacturer Narrative
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An investigation into the reported event has been initiated under (b)(4).Once the investigation has been completed, a follow up report will be submitted with the investigation results and any actions taken by the manufacturer.
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Manufacturer Narrative
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This complaint is recorded by zimmer biomet under (b)(4).No product was returned or pictures provided; visual and dimensional evaluations could not be performed.A definitive root cause cannot be determined.The event cannot be confirmed.The dhr was not reviewed as lot number is required and is not available/provided.If any further information is found which would change or alter any conclusions or information, a supplemental report will be filed accordingly.Zimmer biomet will continue to monitor for trends.
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Event Description
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No additional details regarding the event are available.
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Event Description
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It was reported that during testing, the device was leaking air and spontaneously deflated.The device was brand new.The patient was under anesthesia during the delay.Due diligence is complete and there is no additional information available.No adverse events were reported as a result of this malfunction.
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Manufacturer Narrative
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This complaint is recorded by zimmer biomet under: (b)(4).If any further information is found which would change or alter any conclusions or information, a supplemental report will be filed accordingly.Zimmer biomet will continue to monitor for trends.
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Search Alerts/Recalls
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