Johnson & Johnson Vision Care recalls ACUVUE OASYS contact lenses with HYDRACLEAR PLUS due to foreign matter complaints between blister and foil. Affected lots expire 05/2020 and 08/2020.
Some contact lenses were associated with complaints of a foreign matter caught between the blister package and foil.
Johnson & Johnson Vision Care is recalling ACUVUE OASYS contact lenses with HYDRACLEAR PLUS after reports of foreign matter getting stuck between the blister package and foil. This could cause discomfort or injury if the lens is not properly handled.
Foreign matter can get caught between the blister package and foil, potentially causing discomfort or injury if the lens is not properly handled. This is a packaging issue, not a defect in the lens itself.
Contact lens wearers who purchased ACUVUE OASYS lenses with HYDRACLEAR PLUS between the specified lots. People with sensitive eyes or frequent lens users are at slightly higher risk.
Check for lot numbers L002NCS (expires 05/2020) or L002QH9 (expires 08/2020) on the packaging. The lenses have a base curve of 8.8 and refractive power of -4.00D or -4.50D.
Look for lot numbers L002NCS (expires 05/2020) or L002QH9 (expires 08/2020) on the packaging.
Foreign matter can get caught between the blister package and foil, potentially causing discomfort or injury.
No, but you should check your packaging for the lot numbers and contact Johnson & Johnson Vision Care if you have the affected lot numbers.
Check for lot numbers L002NCS (expires 05/2020) or L002QH9 (expires 08/2020) on the packaging. The lenses have a base curve of 8.8 and refractive power of -4.00D or -4.50D.
We’ve drafted a message you can send Johnson & Johnson Vision Care to request your refund or repair — edit it as you like.
Subject: Recall Z-1209-2018 — Johnson & Johnson Vision Care Johnson & Johnson Vision Care Hello, I own a Johnson & Johnson Vision Care that is covered by recall Z-1209-2018 from Johnson & Johnson Vision Care. 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.
