Drug recall
Risperdal (Risperidone) Tablets, 3 mg, 60 count bottles, Rx only, Janssen Pharmaceutical Products, LP…
FDA recall event 29042 · Class II · Top Rx
Key facts
| Event ID | 29042 |
|---|---|
| Recall numbers | D-251-4 |
| Recalling firm | Top Rx |
| Product type | Drugs |
| Products | Risperdal (Risperidone) Tablets, 3 mg, 60 count bottles, Rx only, Janssen Pharmaceutical Products, LP. Titusville, NJ 08560, NDC 50458-33006 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Adulterated; Presence of Foreign Tablets |
| Initiation date | May 4, 2004 |
| City | Bartlett |
| Country | United States |
| FEI number | 1053152 |
At a glance
- 1–9 Products in this recall
- 1–9 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