Drug recall

HNA Classic 306 Patient Manager Blood Bank Software

FDA recall event 31279 · Class II · Cerner Corporation

Key facts

Event ID 31279
Recall numbers B-0843-5
Recalling firm Cerner Corporation
Product type Biologics
Products HNA Classic 306 Patient Manager Blood Bank Software
Classification Class II
Status Ongoing
Voluntary or mandated Firm Initiated
Reason for recall Defects in the design of blood bank software could result in loss of patient antibody information.
Initiation date Feb 25, 2005
City Kansas City
Country United States
FEI number 1931259

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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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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