Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 87785 · Class II · Medic Inc

Key facts

Event ID 87785
Recall numbers B-0402-2021
Recalling firm Medic Inc
Product type Biologics
Products Blood and Blood Products for Reprocessing
Classification Class II
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Blood product, collected from an unsuitable donor due to a donor screening deviation, was distributed.
Initiation date Mar 26, 2021
Report date May 26, 2021
Termination date May 18, 2021
City Knoxville
State TN
Country United States
FEI number 1077605

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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