Drug recall

Platelets

FDA recall event 81370 · Class II · Carter BloodCare

Key facts

Event ID 81370
Recall numbers B-0076-2019
Recalling firm Carter BloodCare
Product type Biologics
Products Platelets
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from a donor who traveled to a malarial endemic area, was distributed.
Initiation date Sep 24, 2018
Report date Nov 7, 2018
Termination date Oct 30, 2018
City Bedford
State TX
Country United States
FEI number 3002603147

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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