Alprazolam 1 mg Tablets — Class II drug recall D-1153-2014
Terminated recall by Actavis Elizabeth LLC, reported 2014-03-19, distributed nationwide. Failed Tablet/Capsule Specifications: Complaints were received for significant tablet erosion for Alprazolam 1
| Recall number | D-1153-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Actavis Elizabeth LLC, Elizabeth, NJ, United States |
| Recall initiated | 2014-02-10 |
| Classified | 2014-03-10 |
| Reported by FDA | 2014-03-19 |
| Terminated | 2014-08-25 |
| Distributed | Nationwide (US) |
| Quantity | 9,447 bottles |
| NDC | 00228-2027, 00228-2027-10, 00228-2027-50, 00228-2027-96, 00228-2029, 00228-2029-10, 00228-2029-50, 00228-2029-96, 00228-2031, 00228-2031-10, 00228-2031-50, 00228-2031-96, 00228-2039, 00228-2039-10 |
| Lot numbers | 1826E131 |
| Expiration dates | 2015-04 |
Product
Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only , C IV, Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue Elizabeth, NJ 07207 USA, NDC 0228-2031-50
Reason for recall
Failed Tablet/Capsule Specifications: Complaints were received for significant tablet erosion for Alprazolam 1 mg.
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-1153-2014. 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.