FDA Adverse Event
Malfunction
Summary report: N
PALL POSIDYNE ELD SET SAVER
MDR report key: 220550
·
Received April 23, 1999
Report
- Report Number
- 2432733-1999-00004
- Event Type
- Malfunction
- Date Received
- April 23, 1999
- Date of Event
- February 1, 1999
- Report Date
- March 25, 1999
- Manufacturer
- PALL BIOMEDICAL PRODUCTS CO.
- Product Code
- FPB
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TW
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT A LEAK WAS OBSERVED AT THE JOINT BETWEEN THE HOUSING OF THE DEVICE AND TAIL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PALL POSIDYNE ELD SET SAVER | EXTENDED LIFE DISPOSABLE FOR IV THERAPY | FPB | PALL BIOMEDICAL PRODUCTS CO. | ELD96LYLS | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN |