Johnson & Johnson Surgical Vision recalls specific TECNIS Toric II OptiBlue IOL models due to an angle out of specification in the intraocular lens, which may affect alignment during cataract surgery.
Due to intraocular lens containing an angle out of specification (OOS). The cylinder axis marks do not meet product specifications for the allowable angle between Low Power Meridian (LPM) and toric cylinder axis marks.
Johnson & Johnson Surgical Vision is recalling certain TECNIS Toric II OptiBlue IOL models because the lens angle is out of specification. This could lead to improper alignment during cataract surgery, potentially affecting the surgical outcome.
The intraocular lens has an angle that doesn't meet product specifications, which could cause misalignment during cataract surgery. This might lead to improper correction of vision or other surgical complications.
Patients who received the recalled TECNIS Toric II OptiBlue IOL models ZCW during cataract surgery are affected. Those with the specific serial numbers listed are most at risk.
Check if your intraocular lens has the model number ZCW and the listed serial numbers (e.g., 3473902107, 3474002107). These lenses were distributed internationally but not in the U.S.
Reach out to your eye surgeon to confirm if you received a recalled TECNIS Toric II OptiBlue IOL model ZCW with the listed serial numbers.
No, these lenses were not distributed in the U.S. They were sold internationally.
The intraocular lens has an angle out of specification, which could affect alignment during cataract surgery.
Check if your lens has the model number ZCW and one of the listed serial numbers (e.g., 3473902107, 3474002107).
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-0735-2024 — Johnson & Johnson Surgical Vision Johnson & Johnson Surgical Vision Hello, I own a Johnson & Johnson Surgical Vision that is covered by recall Z-0735-2024 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.
