Drug recall

Human Cornea Tissue

FDA recall event 30644 · Class II · Wichita Eye Foundation

Key facts

Event ID 30644
Recall numbers B-0483-5
Recalling firm Wichita Eye Foundation
Product type Biologics
Products Human Cornea Tissue
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Human cornea, collected from a donor who subsequently tested positive for HBsAg by another tissue procurement organization, was distributed.
Initiation date Dec 8, 2004
Termination date Jan 28, 2005
City Wichita
Country United States
FEI number 3001238374

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.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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