FDA recall Z-2646-2023

Product

BD Pyxis MedBank MedPass Software, REF: 139088-01

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 could lead to duplicate medication administration.

Distribution

US: FL, MI, KS

Key facts

Status

Ongoing

Initiation date

2023-08-18

Report date

2023-10-04

Voluntary/Mandated

Voluntary: Firm initiated

Location

San Diego, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2646-2023