Drug recall
Cryoprecipitated AHG
FDA recall event 26546 · Class II · WE & Lela I Stewart Blood Center, Inc
Key facts
| Event ID | 26546 |
|---|---|
| Recall numbers | B-1776-3, B-1777-3 |
| Recalling firm | WE & Lela I Stewart Blood Center, Inc |
| Product type | Biologics |
| Products | Cryoprecipitated AHG, Red Blood Cells |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor who tested reactive for Hepatitis B core antibody (HbcAb) on two occasions, were distributed. |
| Initiation date | Oct 2, 2000 |
| City | Tyler |
| Country | United States |
| FEI number | 1672331 |
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