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FDA (Device enforcement)Recalled 2024-01-15class ii

D.O.R.C. Dutch Opthalmic Research Center Intl B.V.: Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)

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.

Details from the source

Reason for recall: 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. Distribution: US Nationwide distribution in the states of AZ, CO, FL, IN, MD, NC, NY, OH, SC, TX and PR. Quantity: 14 boxes x 6 units per box = 84 units Lot/code info: Product Number: 7223.ALC; UDI/DI: 08717872014173; All lots starting with a number between 2470 and 18705.

UPC codes

08717872014173

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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