Tekia recalls 36 specific Model 872 intraocular lenses with incorrect diopter power labeling. Consumers should check serial numbers to avoid potential vision issues.
A limited number of lenses may be mislabeled with the incorrect diopter power.
Tekia is recalling 36 specific Model 872 intraocular lenses that may have incorrect diopter power labeling. This could lead to improper vision correction if used in surgery.
Lenses with incorrect diopter power could cause improper vision correction during surgery. This is a labeling issue, not a physical defect in the lenses themselves.
Patients who received the recalled lenses during surgery are most at risk. The recall affects only 36 specific serial numbers from a larger batch.
Check the serial number on the lens packaging. The recalled serial numbers include specific combinations starting with U12220229 through V05020831.
Compare your lens serial number to the list of 36 recalled numbers provided in the recall notice.
No, only 36 specific serial numbers from Lot 522-003 are recalled due to incorrect labeling.
Check your serial number against the list of 36 recalled numbers; if it matches, contact Tekia for guidance.
The lenses may have incorrect diopter power labeling, which could lead to improper vision correction during surgery.
We’ve drafted a message you can send Tekia to request your refund or repair — edit it as you like.
Subject: Recall Z-0694-2020 — Tekia Tekia Hello, I own a Tekia that is covered by recall Z-0694-2020 from Tekia. 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.
