OtherLQJ
HGM
Received Mar 26, 1999 · Event occurred Feb 17, 1999
Report 1720381-1999-00004 · MDR key 216744
Device
Generic name
Argon Microfilter
Manufacturer
Fisma, Inc.Model number
K10-A-K03-1-73Catalog number
ZEISS THIN SHUTTER,K3, (MORE)
Lot number
NA
Product problems
- Other (for use when an appropriate device code cannot be identified)
Patient
*
- Other (for use when an appropriate patient code cannot be identified)
Narrative
Description of Event or Problem
PHYSICIAN WAS PERFORMING PROCEDURE USING A ZEISS THIN SHUTTER MICROFILTER WITH AN ARGON LASER. PHYSICIAN NOTICED A MINIMAL AMOUNT OF GREEN LIGHT FLASHBACK. PHYSICIAN PUT ON GOGGLES AND COMPLETED THE PROCEDURE. USER FACILITY REPORTED THAT THERE WAS NO SIGNIFICANT EXPOSURE AND NO FOLLOW-UP DONE ON THEIR PART. THERE WAS NO INJURY TO PHYSICIAN.
Remedial action
- Repair