Drug recall

Whole Blood

FDA recall event 68251 · Class III · Blood Bank Of Delmarva, Inc

Key facts

Event ID 68251
Recall numbers B-0752-14
Recalling firm Blood Bank Of Delmarva, Inc
Product type Biologics
Products Whole Blood
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Whole blood, collected in misbranded collection sets, were distributed.
Initiation date Mar 17, 2014
Report date Jul 2, 2014
Termination date Jun 23, 2014
City Newark
State DE
Country United States
FEI number 2577603

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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