Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 81596 · Class II · OneBlood, Inc.

Key facts

Event ID 81596
Recall numbers B-0168-2019
Recalling firm OneBlood, Inc.
Product type Biologics
Products Blood and Blood Products for Reprocessing
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from an ineligible donor, was distributed.
Initiation date Sep 6, 2018
Report date Nov 28, 2018
Termination date Nov 21, 2018
City St Petersburg
State FL
Country United States
FEI number 1070196

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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