Drug recall
Antihemophilic Factor (Human)
FDA recall event 84254 · Class III · CSL Behring GmbH
Key facts
| Event ID | 84254 |
|---|---|
| Recall numbers | B-0140-2020 |
| Recalling firm | CSL Behring GmbH |
| Product type | Biologics |
| Products | Antihemophilic Factor (Human) |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Lots of Humate-P with misaligned labeling on the folding box, was distributed. |
| Initiation date | Oct 7, 2019 |
| Report date | Dec 4, 2019 |
| Termination date | Nov 25, 2019 |
| City | Marburg |
| Country | Germany |
| FEI number | 3003098680 |
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 · Source date: