Drug recall
Drituss GP Tablets, (Guaifenesin 1200mg and Pseudoephedrine hydrochloride 120mg) 100 count bottles…
FDA recall event 25736 · Class III · Vintage Pharmaceuticals LLC
Key facts
| Event ID | 25736 |
|---|---|
| Recall numbers | D-190-3 |
| Recalling firm | Vintage Pharmaceuticals LLC |
| Product type | Drugs |
| Products | Drituss GP Tablets, (Guaifenesin 1200mg and Pseudoephedrine hydrochloride 120mg) 100 count bottles, Long-Acting, Dye-Free, Rx only, Mfg. for: Qualitest Pharmaceuticals, Inc. Huntsville, AL 35811, Mfg… |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failure to validate manufacturing process |
| Initiation date | Feb 25, 2003 |
| City | Huntsville |
| 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