LUBRICANT EYE DROPS recalled over sterility concerns
- Recall date
- November 13, 2023
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Kilitch Healthcare India Limited recalls LUBRICANT EYE DROPS (Carboxymethylcellulose Sodium 0.5%), packaged 0.5 FL OZ (15mL) bottles (Twin Pack), Distributed by…
- Recall number
- D-0304-2024
- FDA classification
- Class I
- Brand / firm
- Kilitch Healthcare India Limited
- Sold / distributed
- Nationwide within the United States
Why it was recalled
Non-Sterility
Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.
What was recalled
LUBRICANT EYE DROPS (Carboxymethylcellulose Sodium 0.5%), packaged 0.5 FL OZ (15mL) bottles (Twin Pack), Distributed by: Rite Aid 30 Hunter Lane, Camp Hill, PA 17011, NDC 11822-4811-5
Get recall alerts
Free email alert whenever Kilitch Healthcare India Limited has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Kilitch Healthcare India Limited