FDA Adverse Event
Other
Summary report: N
MAXXIM MEDICAL
MDR report key: 144577
·
Received January 14, 1998
Report
- Report Number
- 1035160-1998-00001
- Event Type
- Other
- Date Received
- January 14, 1998
- Report Date
- January 8, 1998
- Manufacturer
- MAXXIM MEDICAL
- Product Code
- LRO
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
PT DEVELOPED EYE IRRITATION FOLLOWING SURGICAL PROCEDURE USING CUSTOM PROCEDURE TRAY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MAXXIM MEDICAL | EYE PACK | LRO | MAXXIM MEDICAL | 6141625 | 01 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN |