Enalapril Maleate Tablet — Class III drug recall D-1683-2012
Terminated recall by Apace KY LLC, reported 2012-09-26, distributed nationwide. Labeling Illegible: Some bottles labels have incomplete NDC numbers and missing strength.
| Recall number | D-1683-2012 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Apace KY LLC, Fountain Run, KY, United States |
| Recall initiated | 2012-09-04 |
| Classified | 2012-09-19 |
| Reported by FDA | 2012-09-26 |
| Terminated | 2013-07-10 |
| Distributed | Nationwide (US) |
| Quantity | 81,516 bottles |
| Reason classes | labeling, potency |
| NDC | 15338-0211-30 |
| Lot numbers | 06/13, DL11600 |
Product
Enalapril Maleate Tablet, USP 5mg 30 Tablet bottle, Rx, Apace Packaging LLC, Ft. Run, KY 42133, NDC 15338-211-30
Reason for recall
Labeling Illegible: Some bottles labels have incomplete NDC numbers and missing strength.
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-1683-2012. 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.