Drug recall
Acellular Dermal Matrix Skin Tissue
FDA recall event 33666 · Class I · LifeCell Corporation
Key facts
| Event ID | 33666 |
|---|---|
| Recall numbers | B-0276-6 |
| Recalling firm | LifeCell Corporation |
| Product type | Biologics |
| Products | Acellular Dermal Matrix Skin Tissue |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Human Tissues, procured from donors without adequate donor eligibility determinations, were distributed. |
| Initiation date | Sep 30, 2005 |
| Termination date | Oct 26, 2010 |
| City | Somerville |
| State | NJ |
| Country | United States |
| FEI number | 1000306051 |
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