FDA Adverse Event
Malfunction
Summary report: N
POLYFLUX LR CAPILLARY DIALYZER
MDR report key: 1010207
·
Received March 10, 2008
Report
- Report Number
- 9611369-2008-00183
- Event Type
- Malfunction
- Date Received
- March 10, 2008
- Date of Event
- November 21, 2007
- Report Date
- February 11, 2008
- Manufacturer
- GAMBRO DIAYLZATOREN GMBH
- Product Code
- MSF
- PMA / PMN Number
- K023615
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- BR
- Reporter Occupation
- NURSE
Narratives
Additional Manufacturer Narrative · 1
INTERNAL BLOOD LEAKS CAN OCCUR DUE TO DAMAGE TO THE HOLLOW FIBRES. NO FURTHER INFO IS EXPECTED FOR THIS SPECIFIC EVENT AND THE CASE IS CONSIDERED CLOSED. THE ROOT CAUSE OF THIS EVENT CANNOT BE DETERMINED. GAMBRO DOES NOT REGARD THE SUBMISSION OF THIS REPORT AS AN ADMISSION OF LIABILITY.
Description of Event or Problem · 1
THE CUSTOMER COMPLAINS ABOUT BLOOD LEAK DURING TREATMENT. THERE WAS INSIGNIFICANT BLOOD LOSS. NO MEDICAL INTERVENTION WAS NEEDED. NO SERIOUS INJURY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | POLYFLUX LR CAPILLARY DIALYZER | MSF | GAMBRO DIAYLZATOREN GMBH | POLYFLUX 8 LR | 7-8203-H-01 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Other |