Drug recall
Bone
FDA recall event 77013 · Class II · AlloSource, Inc.
Key facts
| Event ID | 77013 |
|---|---|
| Recall numbers | B-0523-2017, B-0524-2017 |
| Recalling firm | AlloSource, Inc. |
| Product type | Biologics |
| Products | Bone, Tendon |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Human tissue allografts, processed in a manner that could cause contamination or cross-contamination during processing, as well as the introduction, transmission, or spread of communicable disease… |
| Initiation date | Oct 12, 2016 |
| Report date | Apr 26, 2017 |
| Termination date | Apr 20, 2017 |
| 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: