FDA Device recall Z-0972-2025

BD Pyxis MedStation ES AUX, REF 324

FDA Device
Class II
ongoing
Published 2025-01-29

On 2025-01-29 the FDA classified a Class II recall of BD Pyxis MedStation ES AUX, REF 324 by Carefusion 303, citing 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:….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0972-2025
Classification	Class II
Status	ongoing
Initiated	2023-02-14
Published	2025-01-29
Last updated	2026-09-13 11:57 UTC
Company	Carefusion 303
Distribution	n/a

Product

BD Pyxis MedStation ES AUX, REF 324

Reason

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,

Identifiers

code_info	UDI/DI 10885403512681, Serial Numbers: 9418071, 9418110, 9418124, 9525533, 9525534, 9525559, 9525563, 9525583, 9525601… UDI/DI 10885403512681, Serial Numbers: 9418071, 9418110, 9418124, 9525533, 9525534, 9525559, 9525563, 9525583, 9525601, 9525603, 9525604, 9525607, 9525614, 9525615, 9525616, 9525617, 9525618, 9525629, 9526868, 9528856, 9528857, 9528924, 9528931, 9529144, 9529535, 9530924, 9531251, 9531255, 9531258, 9632432, 9632438, 9632452, 12440840, 12440841, 12448207, 12448208, 12452252, 12452264, 12455476, 12457600, 12457601, 12462734, 12462735, 12463676, 12468607, 12468608, 12468609, 12468610, 12468611, 12468612, 12468670, 12468671, 12468672, 12468673, 12468674, 12473807, 12473808, 12473809, 12473810, 12473811, 12473812, 12473813, 12473815, 12473816, 12473817, 12473887, 12473921, 12473922, 12474012, 12474013, 12474014, 12474015, 12474022, 12474071, 12476548, 12483261, 12483264, 12495456, 12498513, 12498514, 12499285, 12502857, 12502858, 12503069, 12507269, 12507270, 12510393, 12510555, 12510559, 12512134, 12520264, 12520266, 12520267, 12520269, 12528411, 12528519, 12530586, 12530587, 12530588, 12

code_info

UDI/DI 10885403512681, Serial Numbers: 9418071, 9418110, 9418124, 9525533, 9525534, 9525559, 9525563, 9525583, 9525601…

UDI/DI 10885403512681, Serial Numbers: 9418071, 9418110, 9418124, 9525533, 9525534, 9525559, 9525563, 9525583, 9525601, 9525603, 9525604, 9525607, 9525614, 9525615, 9525616, 9525617, 9525618, 9525629, 9526868, 9528856, 9528857, 9528924, 9528931, 9529144, 9529535, 9530924, 9531251, 9531255, 9531258, 9632432, 9632438, 9632452, 12440840, 12440841, 12448207, 12448208, 12452252, 12452264, 12455476, 12457600, 12457601, 12462734, 12462735, 12463676, 12468607, 12468608, 12468609, 12468610, 12468611, 12468612, 12468670, 12468671, 12468672, 12468673, 12468674, 12473807, 12473808, 12473809, 12473810, 12473811, 12473812, 12473813, 12473815, 12473816, 12473817, 12473887, 12473921, 12473922, 12474012, 12474013, 12474014, 12474015, 12474022, 12474071, 12476548, 12483261, 12483264, 12495456, 12498513, 12498514, 12499285, 12502857, 12502858, 12503069, 12507269, 12507270, 12510393, 12510555, 12510559, 12512134, 12520264, 12520266, 12520267, 12520269, 12528411, 12528519, 12530586, 12530587, 12530588, 12

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0972-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.