Model Number 0250080767 |
Device Problem
Break (1069)
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Patient Problems
Foreign Body In Patient (2687); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 02/08/2022 |
Event Type
Injury
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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 a piece of the product broke and remained in the patient.
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Event Description
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It was reported that a piece of the product broke and remained in the patient.
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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: lap instrument broke apart.Probable root cause: use error.Manufacturing/ servicing errors.The reported failure mode will be monitored for future re-occurrence.Manufacture date is not known.H3 other text: 81.
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Search Alerts/Recalls
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