FDA Adverse Event
Injury
Summary report: N
INRATIO
MDR report key: 1853330
·
Received September 30, 2010
Report
- Report Number
- 2027969-2010-01616
- Event Type
- Injury
- Date Received
- September 30, 2010
- Date of Event
- September 14, 2010
- Report Date
- September 30, 2010
- Manufacturer
- ALERE SAN DIEGO, INC.
- Product Code
- GJS
- PMA / PMN Number
- K021923
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
INVESTIGATION PENDING.
Description of Event or Problem · 1
CALLER ALLEGED DISCREPANT RESULTS COMPARED WITH THE LAB. RESULTS AS FOLLOWS: DATE: (B)(6) 2010, INRATIO: 2.3. METER WAS DROPPED BY CLEANING LADY. DATE: (B)(6) 2010, INRATIO: 4.6. PT SKIPPED TWO COUMADIN DOSES AS INSTRUCTED BY DOCTOR. DATE: (B)(6) 2010, INRATIO: 3.8, RE-TEST: 4.4. RE-TEST WAS DONE ON A DIFFERENT FINGER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INRATIO | PROTHROMBIN TIME TEST | GJS | ALERE SAN DIEGO, INC. | 100071 | 221730 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |