Drug recall
PEG-Intron Redipen (Peginterferon alfa-2b), 80mcg/.5mL, For Subcutaneous Use, Rx only, Manufactured by…
FDA recall event 31972 · Class III · Schering Plough Corp
Key facts
| Event ID | 31972 |
|---|---|
| Recall numbers | D-232-5 |
| Recalling firm | Schering Plough Corp |
| Product type | Drugs |
| Products | PEG-Intron Redipen (Peginterferon alfa-2b), 80mcg/.5mL, For Subcutaneous Use, Rx only, Manufactured by Schering Corporation, Kenilworth, NJ 07033, NDC 0085-1316-01 |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Labeling: Needles in the kit have an expiration date that is earlier than the expiration date of the PEG-Intron Redipen itself. |
| Initiation date | Apr 22, 2005 |
| City | Kenilworth |
| Country | United States |
| FEI number | 2210048 |
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