Drug recall
Cartilage
FDA recall event 85281 · Class II · AlloSource, Inc.
Key facts
| Event ID | 85281 |
|---|---|
| Recall numbers | B-0395-2020 |
| Recalling firm | AlloSource, Inc. |
| Product type | Biologics |
| Products | Cartilage |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Human cartilage allografts, which did not meet release criteria designed to prevent contamination or cross-contamination during processing, as well as the introduction, transmission or spread of… |
| Initiation date | Oct 29, 2019 |
| Report date | Apr 1, 2020 |
| Termination date | Mar 20, 2020 |
| City | Centennial |
| State | CO |
| Country | United States |
| FEI number | 3000215346 |
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: