Catalog Number 0377031650 |
Device Problems
Break (1069); Material Split, Cut or Torn (4008)
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Patient Problems
No Consequences Or Impact To Patient (2199); Device Embedded In Tissue or Plaque (3165)
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Event Date 01/16/2020 |
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 the tip of the arthroscopic cannula broke during procedure & pieces potentially remained in joint.Please note that 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 re-opened and the investigation will be updated with new results.Alleged failure: torn arthroscopic cannula probable root cause: poor autoclave reliability use error the reported failure mode will be monitored for future reoccurrence.Manufacture date is not known.
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Event Description
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It was reported that the tip of the arthroscopic cannula broke during procedure & pieces potentially remained in joint.Please note that the procedure was completed successfully.
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Search Alerts/Recalls
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