US Drug Recall Register
Class II · Moderate risk Completed Initiated Jul 2, 2019 (7 years ago)

Ocusoft Goniosoft Hypromellose 2.5% Opthalmic Demulcent Solution, 15 mL, Manufactured…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of Assurance of Sterility

What was recalled

Ocusoft Goniosoft Hypromellose 2.5% Opthalmic Demulcent Solution, 15 mL, Manufactured for: Ocusoft, Inc., Richmond, TX 77406-0429, NDC 54799-503-15

Recalling firm
Altaire Pharmaceuticals, Inc.
NDC code
54799-503-15
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0397-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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