Ocusoft Goniosoft Hypromellose 2.5% Opthalmic Demulcent recall: Sterility Concern
Ocusoft Goniosoft Hypromellose 2.5% Opthalmic Demulcent Solution, 15 mL, Manufactured for: Ocusoft, Inc., Richmond, TX 77406-0429, NDC 54799-503-15
Why was Ocusoft Goniosoft Hypromellose 2.5% Opthalmic Demulcent recalled?
Lack of Assurance of Sterility
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
16260 9/19 17303 10/20 18032 2/21 18235 9/21 18285 11/21 19021 1/22
- Product
- 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.
- Quantity
- N/A
- Distribution
- U.S.A. Nationwide
- Recall date
- November 27, 2019
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (drug)