Leader Dry Eye Relief (10mL) bottles recalled due to non-sterility risk. No remedy specified in official notice.
Non-Sterility
Leader Dry Eye Relief eye drops in 10mL bottles are being recalled because of a non-sterility issue. This could pose a health risk if the product was contaminated during manufacturing.
Non-sterility means the product may have been contaminated with bacteria or other harmful substances during manufacturing. This could lead to infections or other health issues if the eye drops are used.
People who own or use Leader Dry Eye Relief eye drops in 10mL bottles are affected. Those with dry eye conditions may be at higher risk due to the product's intended use.
Check for Leader brand Dry Eye Relief eye drops in 10mL bottles. The product was distributed by Cardinal Health Dublin, Ohio with NDC 70000-0088-1 across all lots.
Identify if you have Leader Dry Eye Relief eye drops in 10mL bottles with NDC 70000-0088-1.
The official notice does not specify any remedy.
The product has a non-sterility issue, meaning it may be contaminated with harmful substances.
Look for Leader brand Dry Eye Relief eye drops in 10mL bottles with NDC 70000-0088-1.
We’ve drafted a message you can send Leader to request your refund or repair — edit it as you like.
Subject: Recall D-0295-2024 — Leader Leader Hello, I own a Leader that is covered by recall D-0295-2024 from Leader. 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.
