FDAMay 9, 2018device

OptiMedica Catalys Precision Laser System, CE 0044 containing software cOS 5.00.33 Product Label for Serial Numbers: 44109015; 44106215; 44107315; and 44065613 label states "Manufactured for: OptiMedica Corporation 1310 Moffett Park Drive Sunnyvale, CA 94089 USA Product Label for Serial Numbers: ...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Software upgrade exhibits failures when executing Daily Alignment Verification (DAV), specifically, cuts on the plastic hemisphere during DAV do not match the intended cuts shown on the treatment overlay screen on the system GUI.

What to do

FDA enforcement status: Terminated

Brands named

johnson johnson surgical visionjohnsonjohnson johnson

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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