Catalog Number 0250070620 |
Device Problems
Fracture (1260); Material Separation (1562)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 04/02/2023 |
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 a piece of the saline bag fell inside the patient.Please note that the piece was removed and the procedure was completed successfully.
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Event Description
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It was reported that a piece of the saline bag fell inside the patient.Please note that the piece was removed and the procedure was completed successfully.
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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: foreign body lodged in the abdominal cavity probable root cause: 1.Material/design error.2.Manufacturing/assembly/ service error.3.Excessive user force.4.Severe shipping conditions.5.Disposable tip rubbing against product.6.User error.The reported failure mode will be monitored for future reoccurrence.
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Search Alerts/Recalls
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