CooperVision recalls specific contact lens models due to incorrect power. Affected lenses may not provide proper vision correction, potentially causing discomfort or vision issues.
Incorrect power of lenses than the expected
CooperVision is recalling certain contact lenses that have incorrect power levels. This could lead to improper vision correction and discomfort for users. The recall affects specific lot numbers of the Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 lenses.
The lenses have incorrect power levels compared to what was expected. This can result in improper vision correction, causing discomfort or vision issues for users who rely on these lenses for extended wear.
Contact lens wearers who purchased the specific lot numbers of CooperVision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 lenses (extended wear) are affected. Those with vision correction needs should check if their lenses match the recalled model.
Check for lot numbers 15628000006509 or 15628000007509 on the packaging of CooperVision Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 soft contact lenses (extended wear).
Look for lot numbers 15628000006509 or 15628000007509 on the packaging of the contact lenses.
The recall indicates the lenses have incorrect power levels, which could cause vision issues. Affected users should stop using them and contact CooperVision for a replacement.
Check the lot numbers on the packaging: 15628000006509 or 15628000007509 for the specific Vertex Toric /2 Clear Toric- Power +2.25 -0.75/120 lenses.
Contact CooperVision directly to get a replacement or refund for the affected lot numbers.
We’ve drafted a message you can send CooperVision to request your refund or repair — edit it as you like.
Subject: Recall Z-1228-2020 — CooperVision CooperVision Hello, I own a CooperVision that is covered by recall Z-1228-2020 from CooperVision. 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.
