Drug recall
Qualitest¿, Butalbital and Acetaminophen Tablets, 50mg/325mg, 100 Tablets, Rx only, NDC 0603-2540-21, Mfg for…
FDA recall event 50116 · Class III · Mikart Inc
Key facts
| Event ID | 50116 |
|---|---|
| Recall numbers | D-139-2009 |
| Recalling firm | Mikart Inc |
| Product type | Drugs |
| Products | Qualitest¿, Butalbital and Acetaminophen Tablets, 50mg/325mg, 100 Tablets, Rx only, NDC 0603-2540-21, Mfg for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35800; Mfg by: Mikart, Inc., Atlanta, GA… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | May contain some low weight tablets. |
| Initiation date | Oct 23, 2008 |
| Termination date | Nov 3, 2009 |
| City | Atlanta |
| State | GA |
| Country | United States |
| FEI number | 1050658 |
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