FDA Recall D-0500-2026

Thea Pharma, Inc. · Waltham, MA

Class II Ongoing 21 days on record

Moderate impact — Class II recall — temporary or medically reversible adverse health consequence possible; remote probability of serious adverse health consequence.

Product

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 82584-700-11

Lot / code: Lot#: 3T36B, Exp. Date October 31, 2026.

Reason for recall

Lack of Assurance of Sterility: This recall has been initiated due to CGMP deviations found by the FDA during an inspection of the manufacturer.

Recall record

Recall number: D-0500-2026
Classification: Class II
Status: Ongoing
Voluntary or mandated: Voluntary: Firm initiated
Firm notification: Letter
Distribution: Nationwide within the United States
Recall initiated: 2026-04-23
Classified by FDA Center: 2026-04-28
FDA published: 2026-05-06
Recalling firm: Thea Pharma, Inc.
Firm location: Waltham, MA

Drug identification

Brand name(s): IVIZIA DRY EYE
Generic name(s): POVIDONE
Manufacturer(s): Thea Pharma Inc.
NDC(s): 82584-700
Route(s): OPHTHALMIC

Operational response

Class II recalls indicate possible temporary or reversible health consequences. Remove affected lots from active dispensing. Segregate inventory. Check the firm’s recall notification for guidance on patient outreach.

For the official FDA enforcement record, see FDA's Recall Search.

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