Drug recall
ALLOPURINOL TABLETS, USP, 300 mg, 500 count bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS…
FDA recall event 71776 · Class III · Qualitest Pharmaceuticals
Key facts
| Event ID | 71776 |
|---|---|
| Recall numbers | D-1405-2015 |
| Recalling firm | Qualitest Pharmaceuticals |
| Product type | Drugs |
| Products | ALLOPURINOL TABLETS, USP, 300 mg, 500 count bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811 --- NDC 0603-2116-28 |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failed Tablet/Capsule Specifications; report of oversized and discolored tablets |
| Initiation date | Jul 20, 2015 |
| Report date | Sep 9, 2015 |
| Termination date | Mar 7, 2016 |
| City | Huntsville |
| State | AL |
| Country | United States |
| FEI number | 1000524784 |
At a glance
- 1–9 Products in this recall
- None 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: