Catalog Number 00882100100 |
Device Problem
Intermittent Loss of Power (4016)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Type
malfunction
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Manufacturer Narrative
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This event has been recorded by zimmer biomet under (b)(4).The investigation is still in progress.Once the investigation is complete a final mdr will be submitted.
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Event Description
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It was reported that the product works intermittently.It is not fast enough and impossible to use it in this condition.No adverse events were reported as a result of this malfunction.
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Manufacturer Narrative
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(b)(4).Upon receipt of additional information, it has been determined that this device did not cause or contribute serious injury and has not been previously reported as a serious injury.The initial report was forwarded in error and should be voided.
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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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