Drug recall

Cryoprecipitated AHF

FDA recall event 40953 · Class II · American Red Cross Blood Services

Key facts

Event ID 40953
Recall numbers B-0623-13
Recalling firm American Red Cross Blood Services
Product type Biologics
Products Cryoprecipitated AHF
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from a donor whose suitability to donate was not adequately determined, was distributed.
Initiation date Oct 4, 2005
Report date Feb 20, 2013
Termination date Feb 11, 2013
City Saint Louis
State MO
Country United States
FEI number 1973035

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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