Class II

Medical Device Recall: Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)

D.O.R.C. Dutch Opthalmic Research Center Intl B.V. · January 15, 2024

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.

States Affected

NATIONWIDE

Quantity Affected

14 boxes x 6 units per box = 84 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1331-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.