Catalog Number EMC9601N |
Device Problem
Air/Gas in Device (4062)
|
Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
|
Event Type
malfunction
|
Event Description
|
It was reported that a buretrol blood administration set had air in the line.This was identified during use.There was no report of patient injury or medical intervention associated with this event.No additional information is available.
|
|
Manufacturer Narrative
|
E1: initial reporter address (b)(6).Should additional relevant information become available, a supplemental report will be submitted.
|
|
Manufacturer Narrative
|
H10: 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
|