Catalog Number P2000 |
Device Problem
Pressure Problem (3012)
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Patient Problems
Peritoneal Laceration(s) (2003); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 03/09/2023 |
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 an additional procedure was performed on 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.Please note stryker is not the legal manufacturer of the device on this investigation.Alleged failure: fluid in the abdomen.Probable root cause: incorrect procedure selection, or insufficient fluid pressure or flow, compromising visibility.The reported failure mode will be monitored for future reoccurrence.
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Event Description
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It was reported that an additional procedure was performed on the patient.
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Search Alerts/Recalls
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