Johnson & Johnson Surgical Vision recalls TECNIS Eyhance IOLs (REF: ICB00, STERILE.EO) due to potential unintended toric fiducial marks. Affected patients should contact the company for details.
Their is a potential that intraocular lenses (IOLs) were manufactured with unintended toric fiducial marks.
Johnson & Johnson Surgical Vision has recalled certain TECNIS Eyhance IOLs because they may have unintended toric fiducial marks. This could affect the lens's alignment during surgery, potentially leading to vision issues after implantation.
The IOLs may have unintended toric fiducial marks, which are small alignment markers used during surgery. If these marks are not properly aligned, the lens might not function correctly after implantation, potentially causing vision problems.
Patients who received the recalled TECNIS Eyhance IOLs (REF: ICB00, STERILE.EO) from Johnson & Johnson Surgical Vision. Those with the specific serial numbers listed in the recall are most at risk.
Check if your IOL has the serial numbers listed in the recall: 8046642236 through 8047252236. The product is labeled as TECNIS Eyhance IOL, REF: ICB00, STERILE.EO, and requires a prescription (Rx Only).
Compare your IOL's serial number to the list provided in the recall: 8046642236 through 8047252236.
Reach out to Johnson & Johnson Surgical Vision for further instructions on the recall.
The recall is due to a potential presence of unintended toric fiducial marks in the IOLs, which could affect alignment during surgery.
If your IOL has a serial number in the list, contact Johnson & Johnson Surgical Vision for instructions.
Check if your IOL's serial number matches the list: 8046642236 through 8047252236.
We’ve drafted a message you can send Johnson & Johnson Surgical Vision to request your refund or repair — edit it as you like.
Subject: Recall Z-2289-2023 — Johnson & Johnson Surgical Vision Johnson & Johnson Surgical Vision Hello, I own a Johnson & Johnson Surgical Vision that is covered by recall Z-2289-2023 from Johnson & Johnson Surgical Vision. 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.
