Drug recall

Bone

FDA recall event 70380 · Class III · AlloSource, Inc.

Key facts

Event ID 70380
Recall numbers B-0425-15
Recalling firm AlloSource, Inc.
Product type Biologics
Products Bone
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Human bone allografts, mislabeled with an incorrect expiration date, were distributed.
Initiation date Oct 20, 2014
Report date Mar 11, 2015
Termination date Mar 3, 2015
City Centennial
State CO
Country United States
FEI number 3000215346

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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