Johnson & Johnson Surgical Vision recalls TECNIS Toric 1-Piece IOLs with model ZCT150 +23.5D SE 1.50D CYL due to nonconforming intraocular lenses that could pose risks during eye surgery.
Due to the release of nonconforming Intraocular Lenses (IOLs).
Johnson & Johnson Surgical Vision is recalling TECNIS Toric 1-Piece IOLs with model number ZCT150 +23.5D SE 1.50D CYL because they contain nonconforming intraocular lenses. This recall is important because the lenses may not meet safety standards for eye surgery, potentially affecting patient outcomes.
The recall states that the lenses are nonconforming, meaning they do not meet the required safety standards for intraocular lenses used in eye surgery. This could lead to potential complications during or after the procedure, though the exact nature of the risk is not specified in the recall notice.
Patients who have received this specific IOL model during eye surgery are likely affected. Those with the model number ZCT150 +23.5D SE 1.50D CYL are at risk of receiving nonconforming lenses.
Check if your IOL has the model number ZCT150 +23.5D SE 1.50D CYL. The lot number is 8144121847, and the product was intended for placement in the eye during surgery.
Reach out to your eye surgeon to confirm if you received the recalled model of IOL.
The recall states that the lenses are nonconforming, meaning they do not meet the required safety standards for intraocular lenses used in eye surgery.
Check if your IOL has the model number ZCT150 +23.5D SE 1.50D CYL with lot number 8144121847.
Contact your eye surgeon to confirm if you received the recalled model and discuss next steps.
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-1163-2021 — Johnson & Johnson Surgical Vision Johnson & Johnson Surgical Vision Hello, I own a Johnson & Johnson Surgical Vision that is covered by recall Z-1163-2021 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.
