FDAClass II · Drug · Recalled May 20, 2026

Oasis Tears PF recall — Oasis Medical, Inc.

Hazard: 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.

Class II: may cause temporary or medically reversible health consequences.

View the official FDA enforcement record (openFDA) ↗

Official recall ID: D-0525-2026
Brand: Oasis Medical
Classification: Class II
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Description

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.

Affected products

Oasis Tears PF

Companies & origin

Recalling firm location: Glendora, CA, United States
Firm address: 510 S Vermont Ave # 528, 91741-6205

Identifying details (verbatim from the notice)

Product codes / lots: Lot # 1V59, Exp Date: 05/31/26; Lot # 3V12, 3V69, Exp Date: 08/31/26.
Distribution: Nationwide within the United States
Firm notified the public via: Letter
FDA event ID: 98897
Recall initiated: April 27, 2026
FDA classified: May 8, 2026
FDA report date: May 20, 2026

Source: U.S. Food & Drug Administration. This page mirrors the official public-domain record verbatim; the linked government source is authoritative. Source last checked July 24, 2026 at 12:00 AM UTC.

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