Johnson & Johnson Vision Care recalls ACUVUE ADVANCE contact lenses with HYDRACLEAR due to foreign matter complaints between blister and foil. Affected lots include B00DHLP (exp 08/2018) and L002FNL (exp 07/2020).
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 ADVANCE contact lenses with HYDRACLEAR 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 become trapped between the blister package and foil, potentially causing discomfort or injury if the lens is not handled correctly. This is not a serious hazard but may lead to irritation or infection.
Contact lens wearers who purchased ACUVUE ADVANCE lenses with HYDRACLEAR from the listed lots. People with sensitive eyes or frequent lens users are at slightly higher risk.
Check the lot number on the packaging: B00DHLP (expires 08/2018), L002FNL (expires 07/2020), or L002V94 (expires 01/2022). The lenses have a base curve of 8.7 and specific refractive power.
Look for the lot number on the packaging: B00DHLP (exp 08/2018), L002FNL (exp 07/2020), or L002V94 (exp 01/2022).
ACUVUE ADVANCE contact lenses with HYDRACLEAR from lots B00DHLP (exp 08/2018), L002FNL (exp 07/2020), and L002V94 (exp 01/2022).
Some lenses had foreign matter caught between the blister package and foil, causing complaints of discomfort or injury.
No action is required if you have a different lot number. Check your packaging for the specific lot numbers listed in the recall.
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-1210-2018 — Johnson & Johnson Vision Care Johnson & Johnson Vision Care Hello, I own a Johnson & Johnson Vision Care that is covered by recall Z-1210-2018 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.
