|
Device Problems
Filling Problem (1233); Improper Flow or Infusion (2954); No Flow (2991)
|
Patient Problem
No Consequences Or Impact To Patient (2199)
|
Event Type
malfunction
|
Manufacturer Narrative
|
Should additional relevant information become available, a supplemental report will be submitted.
|
|
Event Description
|
It was reported an unknown quantity of unspecified access sets were observed to have under infused up to 25%, air in the lines and up stream occlusion alarms when used with sigma spectrum iq infusion pump.There was no report of patient injury or medical intervention associated with this event.No additional information is available.
|
|
Manufacturer Narrative
|
The device was not returned and the lot number is unknown; therefore, a device analysis could not be completed.Should additional relevant information become available, a supplemental report will be submitted.
|
|
Search Alerts/Recalls
|
|
|