FDA Drug recall D-0867-2023
Travoprost Ophthalmic Solution, USP (Ionic Buffered Solution), 0.004%, Rx only, Manufactured by Apotex Inc., Manufactured by: GSMS Incorpor…
- FDA Drug
- Class II
- terminated
- Published 2023-06-14
On 2023-06-14 the FDA classified a Class II recall of Travoprost Ophthalmic Solution, USP (Ionic Buffered Solution), 0.004%, Rx only, Manufactured by Apotex Inc., Manufactured by: GSMS Incorpor… by Golden State Medical Supply, citing lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary container.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0867-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2023-05-25 |
| Published | 2023-06-14 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Golden State Medical Supply |
| Distribution | US |
Product
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).
Reason
Lack of Assurance of Sterility: Tamper Evidence Seal is missing on secondary container.
Identifiers
| ndc | 51407-731-25 |
|---|---|
| ndc | 51407-731-05 |
| code_info | Lot #s: a) GS049666, GS049807, Exp: 03/31/2024; b) GS049667, GS051447, Exp: 09/30/2024. |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0867-2023%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.