Directional Laser Probe with Alcon / Lumenis connector — Class II medical device recall Z-1331-2024
Ongoing recall by D.O.R.C. Dutch Opthalmic Research Center Intl B.V., reported 2024-03-27, distributed nationwide. When using those products you may experience difficulties to extend or retract the laser fiber, and in some oc
| Recall number | Z-1331-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | D.O.R.C. Dutch Opthalmic Research Center Intl B.V., Zuidland, Netherlands |
| Recall initiated | 2024-01-15 |
| Classified | 2024-03-21 |
| Reported by FDA | 2024-03-27 |
| Distributed | Nationwide (US) |
| UPC / GTIN / UDI-DI | 08717872014173 |
Product
Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1331-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.