FDA Adverse Event
Malfunction
Summary report: N
I-STAT CARTRIDGE
MDR report key: 892569
·
Received August 10, 2007
Report
- Report Number
- 2245578-2007-00022
- Event Type
- Malfunction
- Date Received
- August 10, 2007
- Date of Event
- July 6, 2007
- Report Date
- August 10, 2007
- Manufacturer
- ABBOTT POINT OF CARE INC.
- Product Code
- JJE
- PMA / PMN Number
- K894914A
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- BR
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
IN 2007, ABBOTT POINT OF CARE WAS NOTIFIED THAT A CUSTOMER REPORTED A HEMATOCRIT RESULT DISCREPANCY THAT OCCURRED ON ELEVEN DAYS EARLIER. THE CUSTOMER WAS UNABLE TO IDENTIFY WHICH CARTRIDGE TYPE OR CARTRIDGE LOT WAS USED. A HEMATOCRIT RESULT OF 21% PCV WAS OBTAINED FROM THE I-STAT SYSTEM. SINCE THIS RESULT WAS CONSIDERED TO BE NOT COMPATIBLE WITH THE PATIENT'S CLINICAL SITUATION, ANOTHER SAMPLE WAS COLLECTED AND RUN ON A DIFFERENT SYSTEM. THE REPEAT HEMATOCRIT RESULT WAS 36% PCV. NO TREATMENT WAS ADMINISTERED BASED ON THE I-STAT HEMATOCRIT RESULT OF 21% PCV.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | I-STAT CARTRIDGE | IVD | JJE | ABBOTT POINT OF CARE INC. | NA | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | YR |