Staar Surgical recalls EVO VISIAN Implantable Collamer Lenses with specific serial numbers due to potential failure to meet specifications. Consumers should check their lens serial numbers and contact the company for guidance.
Their is a potential that intraocular implant devices may not meet specifications.
Staar Surgical is recalling certain EVO VISIAN Implantable Collamer Lenses because they may not meet required specifications. This could affect the lens's safety and performance in the eye.
The lenses may not meet the required specifications, which could lead to improper function or safety issues in the eye. This is a potential risk but the exact mechanism of failure is not clearly described in the recall notice.
People who have received the recalled EVO VISIAN Implantable Collamer Lenses with the listed serial numbers. Those with the specific serial numbers are most at risk.
Check the serial number on the lens packaging or device. The recalled lenses have specific serial numbers listed in the recall notice, including S1746728, S1713542, S1746725, S1707067, S1734035, S1713494, S1713551, S1740887, and S1713505.
Look for the serial number on the lens packaging or device to determine if it is one of the recalled numbers.
The recall states there is a potential that the intraocular implant devices may not meet specifications, but the exact risk is not clearly described.
Check the serial number on your lens packaging or device against the list provided in the recall notice: S1746728, S1713542, S1746725, S1707067, S1734035, S1713494, S1713551, S1740887, and S1713505.
The recall notice does not specify a remedy, so contact Staar Surgical directly for guidance.
We’ve drafted a message you can send Staar Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-0474-2024 — Staar Surgical Staar Surgical Hello, I own a Staar Surgical that is covered by recall Z-0474-2024 from Staar Surgical. 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.
