Bausch & Lomb recalls enVista one-piece hydrophobic acrylic toric intraocular lenses with misaligned toric axis marks that could affect surgical outcomes after cataract removal.
The toric axis marks were misaligned (from the expected position in relation to the haptics) on an implanted lens.
Bausch & Lomb is recalling enVista one-piece hydrophobic acrylic toric intraocular lenses due to misaligned toric axis marks on implanted lenses. This could lead to improper alignment during cataract surgery, potentially affecting visual correction results.
The toric axis marks on the lens were misaligned relative to the haptics (the parts that hold the lens in place). This misalignment could cause the lens to be positioned incorrectly after surgery, potentially affecting visual correction.
Adult patients who received the recalled enVista lenses during cataract surgery. Patients with the specific lot and serial numbers listed in the recall are most at risk.
Check if your lens has the lot number 3043212 and serial numbers 3043212002 through 3043212008. These lenses were used for cataract surgery in adults to correct vision.
Verify your lens has the lot number 3043212 and serial numbers 3043212002 to 3043212008.
The toric axis marks were misaligned relative to the haptics on the implanted lens, which could affect visual correction after cataract surgery.
Check if your lens has the lot number 3043212 and serial numbers 3043212002 through 3043212008. If you do, contact Bausch & Lomb for further instructions.
The recall addresses potential surgical misalignment, not a risk of injury during normal use. The hazard is specific to the surgical procedure.
We’ve drafted a message you can send Bausch & Lomb to request your refund or repair — edit it as you like.
Subject: Recall Z-2552-2020 — Bausch & Lomb Bausch & Lomb Hello, I own a Bausch & Lomb that is covered by recall Z-2552-2020 from Bausch & Lomb. 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.
