Drug recall
Alprazolam 1 mg Tablets, USP, 500 count Bottle, Rx Only, C IV, Manufactured by: Actavis Elizabeth LLC 200…
FDA recall event 67519 · Class II · Actavis Elizabeth LLC
Key facts
| Event ID | 67519 |
|---|---|
| Recall numbers | D-1153-2014 |
| Recalling firm | Actavis Elizabeth LLC |
| Product type | Drugs |
| Products | 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 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Tablet/Capsule Specifications: Complaints were received for significant tablet erosion for Alprazolam 1 mg. |
| Initiation date | Feb 10, 2014 |
| Report date | Mar 19, 2014 |
| Termination date | Aug 25, 2014 |
| City | Elizabeth |
| State | NJ |
| Country | United States |
| FEI number | 2211563 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: