Lisinopril Tablets USP — Class III drug recall D-1036-2016
Terminated recall by Sandoz Inc, reported 2016-06-22, distributed nationwide. Labeling: Incorrect or Missing Package Insert
| Recall number | D-1036-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sandoz Inc, Princeton, NJ, United States |
| Recall initiated | 2016-05-25 |
| Classified | 2016-06-16 |
| Reported by FDA | 2016-06-22 |
| Terminated | 2017-04-25 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| NDC | 00185-0630-01 |
| Lot numbers | 02/18, FC1960 |
Product
Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0185-0630-01
Reason for recall
Labeling: Incorrect or Missing Package Insert
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-1036-2016. 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.