Model Number 0250080321 |
Device Problem
Break (1069)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 02/09/2022 |
Event Type
malfunction
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Manufacturer Narrative
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Additional information will be provided once the investigation has been completed.The device manufacturer date is not known at this time.However, should it become available it will be provided in future reports.
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Event Description
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It was reported that the device breaking inside the patient.The broken piece was removed.
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Event Description
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It was reported that the device breaking inside the patient.The broken piece was removed.
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Manufacturer Narrative
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This complaint investigation was closed based on the device not received, therefore the reported failure mode was not confirmed.In the event that the device is received, the complaint will be reopened and the investigation will be updated with new results.Alleged failure: babrock broken probable root cause: use error manufacturing/ servicing errors the reported failure mode will be monitored for future reoccurrence.Manufacture date is not known.H3 other text : 81.
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Search Alerts/Recalls
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