FDA recall Z-0972-2025

Product

BD Pyxis MedStation ES AUX, REF 324

Reason for recall

Drawer and/or door failures that may lead to a delay in access to medications. The following three situations in which drawer and/or door failures may occur have been identified: Situation 1: Door Latch Failure, Situation 2: Cable Ribbon Damage, Situation 3: Magnet Falling Out,

Distribution

Worldwide

Key facts

Status

Ongoing

Initiation date

2023-02-14

Report date

2025-01-29

Voluntary/Mandated

Voluntary: Firm initiated

Location

San Diego, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0972-2025