Cardinal Health recalls LEADER Lubricant Eye Drops (0.5% Carboxymethylcellulose Sodium) due to non-sterility found at manufacturing facility. All lots affected.
Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
Cardinal Health is recalling all LEADER Lubricant Eye Drops (0.5 fl oz) because the FDA found bacterial contamination during production. Using these drops could lead to eye infections or other health issues.
The FDA found bacterial contamination in the manufacturing facility, meaning the drops may not be sterile. This could cause eye infections or other infections if used.
People who own or use LEADER Lubricant Eye Drops (0.5 fl oz) are affected. Those with sensitive eyes or frequent users are at higher risk.
Check for LEADER brand Lubricant Eye Drops (0.5 fl oz) dropper bottles with NDC 70000-0090-1. All lots were affected.
Look for the LEADER brand, 0.5 fl oz dropper bottles, and NDC 70000-0090-1 on the label.
Yes, all lots of LEADER Lubricant Eye Drops (0.5 fl oz) with NDC 70000-0090-1 were recalled.
The recall record does not specify a remedy, so contact Cardinal Health for guidance.
The recall states non-sterility, which could cause eye infections, but the record does not mention serious injury risks.
We’ve drafted a message you can send LEADER to request your refund or repair — edit it as you like.
Subject: Recall D-0133-2024 — LEADER LEADER Hello, I own a LEADER that is covered by recall D-0133-2024 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.
