INRATIO2 PT/INR TEST STRIPS
Report
- Report Number
- 2027969-2015-00854
- Event Type
- Malfunction
- Date Received
- October 16, 2015
- Date of Event
- September 24, 2015
- Report Date
- September 25, 2015
- Manufacturer
- ALERE SAN DIEGO, INC.
- Product Code
- GJS
- PMA / PMN Number
- K110212
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- OTHER
Narratives
INVESTIGATION IS PENDING.
INVESTIGATION/CONCLUSION: IT IS INDICATED THAT THE PRODUCT IS NOT RETURNING FOR EVALUATION. THEREFORE, A REVIEW OF THE ENTIRE IN-HOUSE TESTING HISTORY OF THE REPORTED LOT, K372402, WAS PERFORMED. IN-HOUSE TESTING ON STRIP LOT K372402 MEETS EXPECTATIONS. A REVIEW OF THE MANUFACTURING RECORDS FOR LOT# K372402 DID NOT UNCOVER ANY RELEVANT NON-CONFORMANCES. THE LOT MEETS RELEASE SPECIFICATIONS. ROOT CAUSE COULD NOT BE DETERMINED FROM THE INFORMATION PROVIDED BY THE CUSTOMER. BASED ON THE INFORMATION AVAILABLE, THERE IS NO INDICATION OF A PRODUCT DEFICIENCY. NO CORRECTIVE ACTION IS REQUIRED AT THIS TIME.
A PHYSICIAN'S OFFICE IN (B)(6) ALLEGED A VARIANCE BETWEEN THE INRATIO2 INR RESULT AND THE LABORATORY INR RESULT. RESULTS ARE AS FOLLOWS: INRATIO2 INR: 1.3, LABORATORY INR: 2.3. THERAPEUTIC RANGE: 2.0 - 3.0. THE TIME BETWEEN TESTING WAS THREE (3) MINUTES. THERE WAS NO REPORTED ADVERSE PATIENT SEQUELA. THERE WAS NO ADDITIONAL INFORMATION PROVIDED. (NOTE: THIS MDR FILING IS DUE TO THE DEVICE BEING THE SAME OR SIMILAR AS A DEVICE AVAILABLE IN THE UNITED STATES.)
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 687429 | INRATIO2 PT/INR TEST STRIPS | PROTHROMBIN TIME TEST | GJS | ALERE SAN DIEGO, INC. | 99008G1 | K372402 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |