FDAFDA · Food and drugs·Recall number D-0132-2024
LEADER brand Dry Eye Relief (Carboxymethylcellulose Sodium, 1%); 0.5 FL OZ (15 mL) dropper bottle, Sterile, Distributed By Cardinal Health, Dublin, Ohio. 43017, Made in India NDC: 70000-0089-1
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
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.