Some ORA Carts have the potential to return an incorrect IOL power measurement during cataract surgery. This issue appears to have been caused by a software coding error that results in the lens coefficients for an IOL model being downloaded from the Alcon server in an incorrect order.
Some ORA Carts have the potential to return an incorrect IOL power measurement during cataract surgery. This issue appears to have been caused by a software coding error that results in the lens coefficients for an IOL model being downloaded from the Alcon server in an incorrect order.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Alcon Research, Ltd. to request your refund or repair — edit it as you like.
Subject: Recall Z-3050-2017 — Alcon Research, Ltd. Alcon Research, Ltd. recalls ORA System with VerifEye, Catalog Number 80659983 Hello, I own a Alcon Research, Ltd. recalls ORA System with VerifEye, Catalog Number 8065998300 For use during intraocular lens surgery that is covered by recall Z-3050-2017 from Alcon Research, Ltd.. 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.
