FDA recall Z-0906-2025

CareFusion 303, Inc. · Class II · device

Product

BD Pyxis MedStation ES (Med ES Main), REF: 323; and BD Pyxis MedStation ES (Med ES Main Tower), REF: 352

Reason for recall

Due to an automated dispensing cabinet software issue, when a medication single order contains more than one component and at least one is unavailable for a multi-item or combination order, the order may display as grayed out; alternate location tooltip will display "Server connection failed," not listing other area devices where unavailable item(s) may be found, which may lead to delayed therapy.

Distribution

US Nationwide distribution in the states of NY, NC, LA.

Key facts

Status
Ongoing
Initiation date
2023-04-05
Report date
2025-01-22
Voluntary/Mandated
Voluntary: Firm initiated
Location
San Diego, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0906-2025