Drug recall
CVS¿ pharmacy brand WART REMOVER, MAXIMUM STRENGTH, SALICYLIC ACID, 17% w/w, NET WT. ¿ OZ (14 mL); Over The…
FDA recall event 32650 · Class III · Clay Park Labs Inc
Key facts
| Event ID | 32650 |
|---|---|
| Recall numbers | D-382-5 |
| Recalling firm | Clay Park Labs Inc |
| Product type | Drugs |
| Products | CVS¿ pharmacy brand WART REMOVER, MAXIMUM STRENGTH, SALICYLIC ACID, 17% w/w, NET WT. ¿ OZ (14 mL); Over The Counter, Distributed by CVS Pharmacy, Inc. Woonsocket, RI 02895 |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mislabeled: cartons of CVS pharmacy brand Wart Remover (Liquid) were printed with the Drug Facts Panel referencing Corn Remover (Liquid) |
| Initiation date | Jul 12, 2005 |
| City | Bronx |
| Country | United States |
| FEI number | 2450054 |
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