Drug recall

Apheresis Fresh Frozen Plasma

FDA recall event 78306 · Class III · OneBlood, Inc.

Key facts

Event ID 78306
Recall numbers B-0078-2018
Recalling firm OneBlood, Inc.
Product type Biologics
Products Apheresis Fresh Frozen Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from an ineligible donor, were distributed.
Initiation date Aug 30, 2017
Report date Dec 6, 2017
Termination date Nov 29, 2017
City Orlando
State FL
Country United States
FEI number 1072425

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 · Source date:

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