FDA Device recall Z-1333-2024
Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)
- FDA Device
- Class II
- ongoing
- Published 2024-03-27
On 2024-03-27 the FDA classified a Class II recall of Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm) by D O R C Dutch Opthalmic Research Center Intl B V, citing 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 prec….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1333-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-01-15 |
| Published | 2024-03-27 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | D O R C Dutch Opthalmic Research Center Intl B V |
| Distribution | US |
Product
Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)
Reason
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.
Identifiers
| code_info | Product Number: 7227.ALC; UDI/DI: 08717872031897; All lots starting with a number between 2470 and 18705. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1333-2024%22
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