Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1333-2024 — Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)

U.S. FDA — Device Enforcement · Netherlands · 2024-01-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1333-2024
Date of alert
2024-01-15
Country / jurisdiction
Netherlands
Risk level
Class II
Risk type
recall
Brand
D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
08717872031897
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.