Device Problem
Insufficient Information (3190)
|
Patient Problem
Cardiac Arrest (1762)
|
Event Date 05/12/2014 |
Event Type
Injury
|
Manufacturer Narrative
|
(b)(4).This is one of two device reports related to this event.Additional information has been requested and will be submitted upon receipt accordingly.
|
|
Event Description
|
The plaintiff's attorney alleged the patient experienced a sudden cardiac event shortly after dialysis treatment, which is alleged to have been caused by the product administered during dialysis treatment.
|
|
Manufacturer Narrative
|
This is one of two device reports related to this event.Associated manufacturer report numbers are 1225714-2016-00046 and 1225714-2016-00047.Additional information has been requested and will be submitted upon receipt accordingly.
|
|
Search Alerts/Recalls
|