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Class IIOngoing

Optase Dry Eye Intense Drops (Glycerin 0.2%) recall

FDA recall D-0499-2026 · initiated Apr 20, 2026

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated May 6, 2026How we research

SCOPE HEALTH recalled Optase Dry Eye Intense Drops (Glycerin 0.2%) in Apr 2026 — an FDA Class II recall (D-0499-2026) because Lack of Assurance of Sterility.

May cause temporary or medically reversible harm; low probability of serious harm.

Why it was recalled

Lack of Assurance of Sterility

Sterility could not be assured

The maker could not guarantee the product was sterile. That matters most for injections and eye products, where a contaminated dose reaches past the body's defences.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

Lot#: 8T98, 9T31, 9T32, Exp. Date: 30/04/26; 2V13, 2V14, 2V15, Exp. Date 30/06/26; 3V35, Exp. Date 31/08/26;3V36, 3V37, Exp. Date 30/09/26; 5V45, 5V46, 9V12, Exp. Date 31/03/27; 1X57, 1X70, 1X84, Exp. Date 31/05/27.

Details

Product
Optase Dry Eye Intense Drops (Glycerin 0.2%), packaged in 0.33 fl oz, Sterile, Manufactured for Scope Health Inc., 79 Madison Ave., 8th Floor, New York, NY 10016, USA, NDC 72972-002-01.
Recalling company
SCOPE HEALTH
Classification
Class II
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
Nationwide within the United States
Initiated
Apr 20, 2026
FDA report date
May 6, 2026
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Optase Dry Eye Intense Drops (Glycerin 0.2%) recalled?
SCOPE HEALTH recalled Optase Dry Eye Intense Drops (Glycerin 0.2%) in Apr 2026 — an FDA Class II recall (D-0499-2026) because Lack of Assurance of Sterility. May cause temporary or medically reversible harm; low probability of serious harm.
Why was Optase Dry Eye Intense Drops (Glycerin 0.2%) recalled?
Per the FDA enforcement record, the reason for recall D-0499-2026 was: Lack of Assurance of Sterility
Is a recalled Optase Dry Eye Intense Drops (Glycerin 0.2%) dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. May cause temporary or medically reversible harm; low probability of serious harm. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Optase Dry Eye Intense Drops (Glycerin 0.2%) are affected?
Distributed: Nationwide within the United States. The recall covers these lots — Lot#: 8T98, 9T31, 9T32, Exp. Date: 30/04/26; 2V13, 2V14, 2V15, Exp. Date 30/06/26; 3V35, Exp. Date 31/08/26;3V36, 3V37, Exp. Date 30/09/26; 5V45, 5V46, 9V12, Exp. Date 31/03/27; 1X57, 1X70, 1X84, Exp. Date 31/05/27.. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0499-2026.

Source: openFDA Drug Enforcement record D-0499-2026

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