Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 82137 · Class III · OneBlood, Inc.

Key facts

Event ID 82137
Recall numbers B-0338-2019
Recalling firm OneBlood, Inc.
Product type Biologics
Products Blood and Blood Products for Reprocessing
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor who was previously deferred for taking growth hormone, were distributed.
Initiation date Feb 4, 2019
Report date Feb 27, 2019
Termination date Feb 20, 2019
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.

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:

Browse all FDA drug and product recalls