Drug recall

Pooled Cryoprecipitated AHF

FDA recall event 88717 · Class III · Coastal Bend Blood Center

Key facts

Event ID 88717
Recall numbers B-0614-2021
Recalling firm Coastal Bend Blood Center
Product type Biologics
Products Pooled Cryoprecipitated AHF
Classification Class III
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Pooled Cryoprecipitated AHF, which did not have cryo QC performed, was distributed.
Initiation date Aug 9, 2021
Report date Oct 6, 2021
Termination date Sep 27, 2021
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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