Drug recall

Cryoprecipitated AHF

FDA recall event 70781 · Class II · LifeSource

Key facts

Event ID 70781
Recall numbers B-0500-15
Recalling firm LifeSource
Product type Biologics
Products Cryoprecipitated AHF
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from unsuitable donors, were distributed.
Initiation date Jan 29, 2015
Report date Apr 8, 2015
Termination date Apr 2, 2015
City Rosemont
State IL
Country United States
FEI number 3008744215

At a glance

  • 1–9 Products in this recall
  • 1–9 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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