Model Number N/A |
Device Problems
Fitting Problem (2183); Material Twisted/Bent (2981)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 09/21/2021 |
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 complete, 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 attachment piece of the device was bent preventing it from connecting to the handpiece properly.There was no harm or delay.No adverse events were 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).No product was returned or pictures provided; visual and dimensional evaluations could not be performed.Device is used for treatment.A definitive root cause cannot be determined.The event cannot be confirmed.H3 other text: device not returned.
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Event Description
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No additional event information available.
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Search Alerts/Recalls
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