Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm) Recalled by D.O.R.C. Dutch Opthalmic Research Center Intl B.V. Due to When using those products you may experience difficulties...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact D.O.R.C. Dutch Opthalmic Research Center Intl B.V. directly.
Affected Products
Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)
Quantity: 21 boxes x 6 units each = 126 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report