D.O.R.C. Dutch Opthalmic Research Center Intl B.V.: Medical Device Recall in 2024 - (Recall #: Z-1333-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)

Product Classification:

Class II

Date Initiated: January 15, 2024

Date Posted: March 27, 2024

Recall Number: Z-1333-2024

Event ID: 94022

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.

Status: Ongoing

Product Quantity: 13 boxes x 6 units per box = 78 units

Code Information:

Product Number: 7227.ALC; UDI/DI: 08717872031897; All lots starting with a number between 2470 and 18705.

Distribution Pattern:

US Nationwide distribution in the states of AZ, CO, FL, IN, MD, NC, NY, OH, SC, TX and PR.

Voluntary or Mandated:

Voluntary: Firm initiated