FDA Adverse Event
Malfunction
Summary report: N
CT GAMMA DIALYZER (CT 190G)
MDR report key: 381120
·
Received February 27, 2002
Report
- Report Number
- 1423500-2002-00262
- Event Type
- Malfunction
- Date Received
- February 27, 2002
- Date of Event
- June 5, 2001
- Report Date
- January 28, 2002
- Manufacturer
- NISSHO CORP.
- Product Code
- FJI
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AZ, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
CUSTOMER REPORTS THREE INCIDENTS OF BLOOD LEAKS OCCURRING IN 2001 AT THE ONSET OF PT TREATMENTS. USE NUMBERS RANGED FROM A NEW DIALYZER TO A DIALYZER WITH A REUSE NUMBER OF 5. ALL THE LEAKS WERE NOTED BY BLOOD LEAK ALARMS AND CONFIRMED WITH HEMASTIX. TREATMENTS WERE CONTINUED WITH NEW DIALYZERS AND NEW BLOODLINES WITHOUT INCIDENT. NO PT INJURIES OR MEDICAL INTERVENTIONS WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CT GAMMA DIALYZER (CT 190G) | HOLLOW FIBER DIALYZER | FJI | NISSHO CORP. | CT 190G | E00K06X |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN |