Drug recall
Clonazepam Tablets, USP 2 mg 100 tablets Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue, Elizabeth…
FDA recall event 67053 · Class II · Actavis Elizabeth LLC
Key facts
| Event ID | 67053 |
|---|---|
| Recall numbers | D-1087-2014 |
| Recalling firm | Actavis Elizabeth LLC |
| Product type | Drugs |
| Products | Clonazepam Tablets, USP 2 mg 100 tablets Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue, Elizabeth, NJ 0737 USA NDC 0228-3005-11 packaged in White/Round HDPE 75 CC with white/round plastic… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent Drug: During routine stability testing one tablet was found with tablet weight below specification. |
| Initiation date | Nov 6, 2013 |
| Report date | Mar 5, 2014 |
| Termination date | Jun 2, 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: