Similasan recalled over sterility concerns
- Recall date
- April 23, 2026
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Thea Pharma, Inc. recalls Similasan, iVIZIA, Sterile Lubricant Eye Drops (Povidone 0.5%), 0.33 Fl oz (10 mL), Made in France, Distributed by: The…
- Recall number
- D-0501-2026
- FDA classification
- Class II
- Brand / firm
- Thea Pharma, Inc.
- Sold / distributed
- Nationwide within the United States
Why it was recalled
Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Similasan, iVIZIA, Sterile Lubricant Eye Drops (Povidone 0.5%), 0.33 Fl oz (10 mL), Made in France, Distributed by: Thea Pharma Inc., Waltham, MA 02451, NDC 59262-700-11
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