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FDAJanuary 15, 2024device

Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)

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

The hazard

When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.

What to do

FDA enforcement status: Ongoing

Brands named

d o r c dutch opthalmic research center intl b v

UPCs

08717872014203

Recall history

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

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