FDA Drug recall D-1683-2012
Enalapril Maleate Tablet, USP 5mg 30 Tablet bottle, Rx, Apace Packaging LLC, Ft. Run, KY 42133, NDC 15338-211-30
- FDA Drug
- Class III
- terminated
- Published 2012-09-26
On 2012-09-26 the FDA classified a Class III recall of Enalapril Maleate Tablet, USP 5mg 30 Tablet bottle, Rx, Apace Packaging LLC, Ft. Run, KY 42133, NDC 15338-211-30 by Apace Ky, citing labeling Illegible: Some bottles labels have incomplete NDC numbers and missing strength.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1683-2012 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2012-09-04 |
| Published | 2012-09-26 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Apace Ky |
| Distribution | US |
Product
Enalapril Maleate Tablet, USP 5mg 30 Tablet bottle, Rx, Apace Packaging LLC, Ft. Run, KY 42133, NDC 15338-211-30
Reason
Labeling Illegible: Some bottles labels have incomplete NDC numbers and missing strength.
Identifiers
| code_info | Lot: DL11600 Exp Date: 06/13 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1683-2012%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.