D.O.R.C. recalls Directional Laser Probe with Alcon/Lumenis connector (25 gauge) due to potential difficulties extending or retracting the laser fiber, which may affect precise tip direction during use.
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 Probes with Alcon/Lumenis connectors (25 gauge) because users may have trouble extending or retracting the laser fiber, which could lead to imprecise tip positioning during procedures. This recall affects specific product lots and requires users to check their units for the described issue.
The laser fiber may not extend or retract properly, and the tip may not direct precisely as needed during medical procedures. This could lead to imprecise targeting of the laser beam, potentially affecting treatment outcomes.
Users of the Directional Laser Probe with Alcon/Lumenis connector (25 gauge) for medical procedures are most at risk if they experience difficulty extending or retracting the laser fiber. This recall applies to specific product lots identified by the serial numbers.
Check if your probe has a product number starting with 7225.ALC and a serial number between 2470 and 18705. The product includes a 25 gauge / 0.5 mm connector compatible with Alcon or Lumenis systems.
Verify your probe's product number starts with 7225.ALC and serial number falls between 2470 and 18705.
Users may experience difficulties extending or retracting the laser fiber, and in some cases, may have trouble directing the laser fiber tip precisely.
Check if your probe has a product number starting with 7225.ALC and a serial number between 2470 and 18705.
The recall does not specify a remedy, so contact the manufacturer for further instructions.
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-1332-2024 — D.O.R.C. D.O.R.C. Hello, I own a D.O.R.C. that is covered by recall Z-1332-2024 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.
