Drug recall
Tylenol Allergy Sinus gelcap. Each caplet contains acetaminophen 500 mg, chlorpheniramine maleate 2 mg, and…
FDA recall event 34230 · Class III · McNeil Consumer & Specialty Pharmaceuticals, Division of McN
Key facts
| Event ID | 34230 |
|---|---|
| Recall numbers | D-100-6 |
| Recalling firm | McNeil Consumer & Specialty Pharmaceuticals, Division of McN |
| Product type | Drugs |
| Products | Tylenol Allergy Sinus gelcap. Each caplet contains acetaminophen 500 mg, chlorpheniramine maleate 2 mg, and pseudoephedrine HCl 30 mg, OTC, McNeil Consumer and Specialty Pharmaceuticals, Division of… |
| Classification | Class III |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Defective container: product intended for destruction due a tear in the pouch was possibly diverted to retail stores |
| Initiation date | Sep 19, 2005 |
| City | Fort Washington |
| Country | United States |
| FEI number | 2510184 |
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