DULOXETINE Delayed-Release Capsules — Class III drug recall D-1255-2016
Terminated recall by Golden State Medical Supply Inc., reported 2016-07-20, distributed nationwide. Labeling; Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on container label is 02/2019, c
| Recall number | D-1255-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Golden State Medical Supply Inc., Camarillo, CA, United States |
| Recall initiated | 2016-06-28 |
| Classified | 2016-07-11 |
| Reported by FDA | 2016-07-20 |
| Terminated | 2016-11-28 |
| Distributed | Nationwide (US) |
| Quantity | 2,077 bottles |
| Reason classes | labeling |
| NDC | 60429-0166-10 |
| Lot numbers | GS011709, GS012352 |
Product
DULOXETINE Delayed-Release Capsules, USP, 60 mg, 1000 count bottles, Rx only, Manufactured by: Laboratorios del Dr. Esteve, SA, Martorelles, Barcelona --- NDC 60429-166-10
Reason for recall
Labeling; Incorrect or Missing Lot and/or Exp Date; incorrect expiration date on container label is 02/2019, correct expiration date should be 02/2018
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-1255-2016. 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.