Drug recall
Human Tendon
FDA recall event 79923 · Class I · Aziyo Biologics
Key facts
| Event ID | 79923 |
|---|---|
| Recall numbers | B-0659-2018 |
| Recalling firm | Aziyo Biologics |
| Product type | Biologics |
| Products | Human Tendon |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Distribution of human tissue allografts, that could cause contamination or cross-contamination during processing, as well as the introduction, transmission, or spread of communicable disease through… |
| Initiation date | Jan 10, 2018 |
| Report date | Jul 18, 2018 |
| Termination date | Jul 12, 2018 |
| City | Richmond |
| State | CA |
| Country | United States |
| FEI number | 1000100754 |
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 · Source date: