Oasis Medical, Inc. recalls Oasis Tears PF
- Recalling company
- Oasis Medical, Inc.
- Product
- Oasis Tears PF, Preservative-Free Lubricant Eye Drops, 10mL/0.34 Fl OZ Bottle, Sterile, Manufactured for: OASIS Medical, Inc., 514 S. Vermont Ave., Glendora, CA 91741, USA, Made in France, NDC 42126-6400-1.
- Reason
- Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of Excelvision.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Apr 27, 2026
- Reported
- May 20, 2026
- Distribution
- Nationwide within the United States
- Status
- Ongoing
- Lot / codes
- Lot # 1V59, Exp Date: 05/31/26; Lot # 3V12, 3V69, Exp Date: 08/31/26.
- Company location
- Glendora, CA
- Recall type
- Voluntary: Firm initiated
- Recall number
- D-0525-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number D-0525-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.