D.O.R.C. recalls Directional Laser Probe with Alcon/Lumenis connector (23 gauge) due to difficulty extending or retracting the laser fiber, potentially affecting precise tip direction.
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.
D.O.R.C. is recalling Directional Laser Probe devices with Alcon/Lumenis connectors because users may have trouble extending or retracting the laser fiber, which could lead to imprecise tip direction during procedures.
The hazard involves difficulty extending or retracting the laser fiber, which can cause imprecise tip direction during use. This may lead to complications in ophthalmic procedures if the laser fiber is not properly positioned.
Users of the recalled Directional Laser Probe devices, particularly those performing ophthalmic procedures, may be affected. Those with the specific product model and lot numbers are most at risk.
Check for the product model 'Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)' and lot numbers starting with a number between 2470 and 18705.
Identify the product model and lot numbers starting with 2470 to 18705 to confirm if it is recalled.
The recalled model is Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm).
Check for lot numbers starting with a number between 2470 and 18705 on the product label.
The recall record does not specify a remedy, so no action is required beyond checking if your product is affected.
We’ve drafted a message you can send D.O.R.C. to request your refund or repair — edit it as you like.
Subject: Recall Z-1331-2024 — D.O.R.C. D.O.R.C. Hello, I own a D.O.R.C. that is covered by recall Z-1331-2024 from D.O.R.C.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
