LightMed USA Inc Model LightLas 532 Opthalmic Photocoagulator Laser Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Model LightLas 532 Opthalmic Photocoagulator Laser
Brand
LightMed USA Inc
Lot Codes / Batch Numbers
All codes
Products Sold
All codes
LightMed USA Inc is recalling Model LightLas 532 Opthalmic Photocoagulator Laser due to Firm needed to include calibration procedures in user guide.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Firm needed to include calibration procedures in user guide.
Recommended Action
Per FDA guidance
Firm fedexed new user manuals with calibration procedures to each consignee on 11/11/2003.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, GA
Page updated: Jan 10, 2026