Drug recall

Fresh Frozen Plasma

FDA recall event 86949 · Class II · Coastal Bend Blood Center

Key facts

Event ID 86949
Recall numbers B-0138-2021, B-0139-2021
Recalling firm Coastal Bend Blood Center
Product type Biologics
Products Fresh Frozen Plasma, Red Blood Cells, Leukocytes Reduced
Classification Class II
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Blood products, collected from donors previously deferred for testing reactive for syphilis and who were not properly tested for re-entry, were distributed.
Initiation date Oct 30, 2020
Report date Dec 23, 2020
Termination date Dec 16, 2020
City Corpus Christi
State TX
Country United States
FEI number 1671283

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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