Drug recall
GUAIFEN/PSE tablets, Pseudoephedrine HCl 120mg, Guaifenesin 600mg, 100 count bottles, Rx Only, Mfg. for…
FDA recall event 25530 · Class III · Vintage Pharmaceuticals LLC
Key facts
| Event ID | 25530 |
|---|---|
| Recall numbers | D-159-3 |
| Recalling firm | Vintage Pharmaceuticals LLC |
| Product type | Drugs |
| Products | GUAIFEN/PSE tablets, Pseudoephedrine HCl 120mg, Guaifenesin 600mg, 100 count bottles, Rx Only, Mfg. for QUALITEST PHARMACEUTICALS, INC., HUNTSVILLE, AL 35811, Mfg. by VINTAGE PHARMACEUTICALS, LLC… |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Content Uniformity failure for PSE |
| Initiation date | Jan 16, 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