Emtriva — Class II drug recall D-0045-2015
Terminated recall by Gilead Sciences, Inc., reported 2014-11-05, distributed in PR. Defective Container; leaking around the cap
| Recall number | D-0045-2015 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Gilead Sciences, Inc., Foster City, CA, United States |
| Recall initiated | 2014-10-01 |
| Classified | 2014-10-24 |
| Reported by FDA | 2014-11-05 |
| Terminated | 2015-05-11 |
| Distributed | PR |
| Quantity | 6,290 bottles |
| Reason classes | packaging |
| NDC | 61958-0601, 61958-0601-01, 61958-0602, 61958-0602-01 |
| Lot numbers | HDNTD1 |
| Expiration dates | 2015-06-30, 2015-10-31, 2016-04-30, 2016-10-31 |
Product
Emtriva (emtricitabine) Oral Solution, 10 mg/mL, 170 mL bottles, Rx only, Manufactured for Gilead Sciences, Inc., Foster City, CA NDC 61958-0602-1 Gilead Sciences, Inc. Foster City, CA 94404.
Reason for recall
Defective Container; leaking around the cap
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-0045-2015. 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.