Fresh Recalls

FDAClass II · Drug · Recall D-0525-2026 · Recalled May 20, 2026

Oasis Tears PF recall — Oasis Medical, Inc.

Agency report date: May 20, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Oasis Tears PF
Company / brand
Oasis Medical
Lot / serial / date codes
Lot # 1V59, Exp Date: 05/31/26; Lot # 3V12, 3V69, Exp Date: 08/31/26.
Distribution
Nationwide within the United States
Agency product description and boundaries

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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

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

Affected product: Oasis Tears PF recall status

3. Open the official notice or contact

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

Affected products

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

Other drug recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved August 18, 2026 at 6:00 PM UTC.

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