Ocusoft Goniosoft Hypromellose 2.5% Opthalmic Demulcent Solution, 15 mL, Manufactured for: Ocusoft, Inc., Richmond, TX 77406-0429, NDC 54799-503-15
Reported: November 27, 2019 Initiated: July 2, 2019 #D-0397-2020
Product Description
Ocusoft Goniosoft Hypromellose 2.5% Opthalmic Demulcent Solution, 15 mL, Manufactured for: Ocusoft, Inc., Richmond, TX 77406-0429, NDC 54799-503-15
Reason for Recall
Lack of Assurance of Sterility
Details
- Recalling Firm
- Altaire Pharmaceuticals, Inc.
- Units Affected
- N/A
- Distribution
- U.S.A. Nationwide
- Location
- Aquebogue, NY
Frequently Asked Questions
What product was recalled? ▼
Ocusoft Goniosoft Hypromellose 2.5% Opthalmic Demulcent Solution, 15 mL, Manufactured for: Ocusoft, Inc., Richmond, TX 77406-0429, NDC 54799-503-15. Recalled by Altaire Pharmaceuticals, Inc.. Units affected: N/A.
Why was this product recalled? ▼
Lack of Assurance of Sterility
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 27, 2019. Severity: Moderate. Recall number: D-0397-2020.
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