FDAFDA · Food and drugs·Recall number D-0135-2024
LEADER brand Dry Eye Relief (Polyethylene Glycol 400, 0.4% Propylene Glycol, 0.3%); 0.33 FL OZ (10 mL) dropper bottle, Sterile, Distributed By Cardinal Health, Dublin, Ohio 43017, Made in India NDC: 70000-0088-1
Published November 29, 2023 · Recall initiated: October 31, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Brand
- DRY EYE RELIEF
- Manufacturer
- Cardinal Health Inc.
- Distributor
- Nationwide in the USA
- Lot
- ALL LOTS
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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