|
Model Number 7211004 |
Device Problems
Increase in Pressure (1491); Connection Problem (2900)
|
Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
|
Event Date 01/01/1901 |
Event Type
malfunction
|
Event Description
|
It was reported that, during a acl surgery, three (3) dyonics 25 cartridge tubing sets were not sitting properly in the pump so the pump is over pumping fluid.The cartridge could be manually pushed in further to solve the issue but came back out as soon as it is not being pushed.Surgery was resumed, after a non-significant delay, with a back-up device.No patient complications were reported.
|
|
Manufacturer Narrative
|
Internal complaint reference: case (b)(4).
|
|
Manufacturer Narrative
|
H3, h6: the reported device was not returned to the designated complaint unit for independent evaluation, thus visual inspection and functional testing could not be performed.A review of device records showed there were no indications to suggest that the product did not meet manufacturing specification upon release for distribution.A complaint history review found similar reported events.A risk management review found that the reported failure and/or harm was documented appropriately, and there were no indications to suggest the anticipated risk is not adequate.There was no relationship found between the device and the reported event.The complaint was not confirmed.Please refer to the instructions for use for recommendations on proper use of the device and potential troubleshooting methods to prevent future reoccurrence of the reported event.No containment or corrective actions are recommended at this time.If the product associated with this event is returned at a future date, this investigation will be reopened for evaluation.
|
|
Search Alerts/Recalls
|
|
|