FDA Adverse Event
Malfunction
Summary report: N
INRATIO
MDR report key: 2070801
·
Received April 15, 2011
Report
- Report Number
- 2027969-2011-00854
- Event Type
- Malfunction
- Date Received
- April 15, 2011
- Date of Event
- March 25, 2011
- Report Date
- April 15, 2011
- Manufacturer
- ALERE SAN DIEGO, INC
- Product Code
- GJS
- PMA / PMN Number
- K021923
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
INVESTIGATION PENDING.
Description of Event or Problem · 1
CALLER ALLEGED DISCREPANT PRECISION RESULTS USING THE INRATIO METER: RESULTS AS FOLLOWS: DATE: (B)(6) 2011, INRATIO: 4.9, RE-TEST: 3.0, RE-TEST: 2.6. ALL TESTS WERE DONE RIGHT ONE AFTER THE OTHER. TESTS WERE DONE ON DIFFERENT FINGERS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INRATIO | PROTHROMBIN TIME TEST | GJS | ALERE SAN DIEGO, INC | 100071 | 243934 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |