FDA Adverse Event
Malfunction
Summary report: N
HIGH SPEED VITRECTOMY CUTTER
MDR report key: 1424259
·
Received March 26, 2009
Report
- Report Number
- 1920664-2009-00077
- Event Type
- Malfunction
- Date Received
- March 26, 2009
- Date of Event
- February 27, 2009
- Report Date
- February 27, 2009
- Manufacturer
- BAUSCH & LOMB
- Product Code
- MLZ
- PMA / PMN Number
- K980488
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
THIS CUTTER FAILED DURING A VITRECTOMY PROCEDURE. THERE WAS NO REPORT OF PATIENT INJURY, AND IT IS LIKELY ANOTHER CUTTER WAS USED TO COMPLETE THE PROCEDURE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HIGH SPEED VITRECTOMY CUTTER | OPHTHALMIC MICROSURGICAL ACCESSORY PACK | MLZ | BAUSCH & LOMB | NA | U0198 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |