Travoprost Ophthalmic Solution USP — Class II drug recall D-0154-2017
Terminated recall by Par Pharmaceutical, Inc., reported 2016-12-07, distributed nationwide. Lack of Assurance of Sterility; damage to the internal portion of the dropper tip portion of the container
| Recall number | D-0154-2017 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Par Pharmaceutical, Inc., Chestnut Ridge, NY, United States |
| Recall initiated | 2016-10-05 |
| Classified | 2016-11-25 |
| Reported by FDA | 2016-12-07 |
| Terminated | 2018-06-18 |
| Distributed | Nationwide (US) |
| Reason classes | sterility |
| Expiration dates | 2016-09, 2016-10, 2016-12, 2017-01, 2017-03, 2017-05, 2017-06, 2017-07, 2017-08, 2017-09, 2017-10 |
Product
Travoprost Ophthalmic Solution USP, 0.004%, a) 2.5 mL and b) 5 mL bottles, Rx only, FOR USE IN THE EYES ONLY, Made in India, Distributed by: Par Pharmaceutical Cos., Inc, Spring Valley, NY 10977
Reason for recall
Lack of Assurance of Sterility; damage to the internal portion of the dropper tip portion of the container
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0154-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.