Drug recall

BD Pyxis MedBank MedPass Software, REF: 139088-01

FDA recall event 92967 · Class II · CareFusion 303, Inc.

Key facts

Event ID 92967
Recall numbers Z-2646-2023
Recalling firm CareFusion 303, Inc.
Product type Devices
Products BD Pyxis MedBank MedPass Software, REF: 139088-01
Classification Class II
Status Ongoing
Voluntary or mandated Firm Initiated
Reason for recall After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which…
Initiation date Aug 18, 2023
Report date Oct 4, 2023
City San Diego
State CA
Country United States
FEI number 2016493

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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