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FDAFDA · Food and drugs·Recall number D-0867-2023

Travoprost Ophthalmic Solution, USP (Ionic Buffered Solution), 0.004%, Rx only, Manufactured by Apotex Inc., Manufactured by: GSMS Incorporated, Camarillo, CA 93012, a) NDC 51407-731-25 (2.5 mL bottle), b) NDC 51407-731-05 (5 mL bottle).

Published June 14, 2023 · Recall initiated: May 25, 2023

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary container.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
TRAVOPROST
Manufacturer
Golden State Medical Supply Inc.
Distributor
Nationwide in the USA
Lot
Lot #s: a) GS049666, GS049807, Exp: 03/31/2024; b) GS049667, GS051447, Exp: 09/30/2024.
Risk classification
Class II
Area (FDA)
drug
Country
United States

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