FDA Adverse Event
Malfunction
Summary report: N
ORTHO SUMMIT PROCESSOR
MDR report key: 486246
·
Received September 16, 2003
Report
- Report Number
- 2250051-2003-01162
- Event Type
- Malfunction
- Date Received
- September 16, 2003
- Date of Event
- September 3, 2003
- Report Date
- September 12, 2003
- Manufacturer
- ORTHO-CLINICAL DIAGNOSTICS
- Product Code
- JTC
- Product Problem
- Yes
- Report Source
- Distributor report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT AFTER PROCESSING AN HBSAG PLATE ON OSP THE PLATE REPORT SHOWED THAT NEGATIVE ODS WERE PRESENT THROUGHOUT ROWS D AND H. NO DEATH OR SERIOUS INJURY WAS ASSOCIATED WITH THIS INCIDENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ORTHO SUMMIT PROCESSOR | SAMPLE PROCESSOR | JTC | ORTHO-CLINICAL DIAGNOSTICS | 7003015 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Other |