Up&Up dry eye relief (0.5% Carboxymethylcellulose) in Twin Packs is recalled due to non-sterility risk. Affected products distributed by Target with NDC 76168-800-30.
Non-Sterility
Up&Up dry eye relief eye drops in Twin Packs are being recalled because of non-sterility. This means the product may not be safe for use and could cause infection.
Non-sterility means the product may contain bacteria or other contaminants that could lead to eye infections. This is a serious health risk when used in the eye.
People who own or use Up&Up dry eye relief eye drops in Twin Packs (0.5 FL OZ bottles) distributed by Target. Those with dry eye conditions are most at risk.
Check for Up&Up dry eye relief eye drops in Twin Packs (0.5 FL OZ bottles) with NDC 76168-800-30. These were distributed by Target stores.
Look for the NDC code 76168-800-30 on the packaging to confirm if your product is affected.
The recall states the product has a non-sterility hazard, meaning it may not be safe for use and could cause eye infections.
Check for Up&Up dry eye relief eye drops in Twin Packs (0.5 FL OZ bottles) with NDC 76168-800-30, distributed by Target.
The recall record does not specify a remedy, so contact the manufacturer or your healthcare provider for guidance.
We’ve drafted a message you can send Up&Up to request your refund or repair — edit it as you like.
Subject: Recall D-0311-2024 — Up&Up Up&Up Hello, I own a Up&Up that is covered by recall D-0311-2024 from Up&Up. 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.
