FDAFebruary 20, 2015device

OptiMedica Catalys Precision Laser System; Model No(s). Catalys-U (US), and Catalys-I (Outside US). Product Usage: Indicated for use in patients undergoing cataract surgery for removal of crystalline lens.

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

The hazard

Device may experience loss of suction during treatment resulting in scoring the cornea during lens fragmentation.

What to do

FDA enforcement status: Terminated

Brands named

abbott medical opticsabbottabbott medical

Recall history

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

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