FDA Adverse Event
Injury
Summary report: N
ALCON SHIELDED BULLET ILLUMINATOR
MDR report key: 3030387
·
Received March 27, 2013
Report
- Report Number
- MW5029549
- Event Type
- Injury
- Date Received
- March 27, 2013
- Report Date
- March 27, 2013
- Manufacturer
- ALCON SURGICAL
- Product Code
- HQB
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- MN, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
HANDLE AND FIBER OPTICS FOR SHIELDED BULLETT ENDO ILLUMINATOR SEPARATE WHILE BEING USED FOR PT CARE. THIS IS THE NINTH TIME THIS HAS OCCURRED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 125303 | ALCON SHIELDED BULLET ILLUMINATOR | SHIELDED BULLET ENDO ILLUMINATOR | HQB | ALCON SURGICAL | 901490M |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |