Oasis Tears PF — Class II drug recall D-0525-2026
Ongoing recall by Oasis Medical, Inc., reported 2026-05-20, distributed nationwide. Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA obs
| Recall number | D-0525-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Oasis Medical, Inc., Glendora, CA, United States |
| Recall initiated | 2026-04-27 |
| Classified | 2026-05-08 |
| Reported by FDA | 2026-05-20 |
| Distributed | Nationwide (US) |
| Reason classes | sterility |
| NDC | 42126-6400, 42126-6400-01 |
| Lot numbers | 1V59, 3V12, 3V69 |
| Expiration dates | 2026-05-31, 2026-08-31 |
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0525-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.