D.O.R.C. recalls Directional Laser Probe with Alcon/Lumenis connector (27 gauge) due to difficulty extending or retracting the laser fiber, potentially affecting precise tip control 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 Probe devices with Alcon/Lumenis connectors that may have trouble extending or retracting the laser fiber, making precise tip control difficult. This could affect medical procedures requiring accurate laser guidance.
The laser fiber may not extend or retract properly, causing the tip to be difficult to direct precisely. This could lead to inaccurate targeting during medical procedures, potentially affecting treatment outcomes.
Medical professionals using the recalled laser probes for eye treatments are most at risk. Patients using these devices for procedures may also be affected if the probe doesn't function as intended.
Check for product number 7227.ALC and Universal Device Identifier (UDI) starting with 08717872031897. The product was sold with lot numbers starting with 2470 to 18705.
Verify the product number (7227.ALC) and lot numbers (2470 to 18705) to confirm if your device is affected.
The recall applies to Directional Laser Probes with Alcon/Lumenis connector (27 gauge / 0.4 mm) and lot numbers starting with 2470 to 18705. Check your product details to confirm.
The recall does not specify a remedy, so no action is required beyond checking if your device is affected.
The hazard description mentions difficulties with fiber extension and precise tip control, but no serious injury risk is stated. This is considered low risk.
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-1333-2024 — D.O.R.C. D.O.R.C. Hello, I own a D.O.R.C. that is covered by recall Z-1333-2024 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.
