FDA Device recall Z-0974-2025

BD Pyxis MedStation 4000 AUX, REF 306

FDA Device
Class II
ongoing
Published 2025-01-29

On 2025-01-29 the FDA classified a Class II recall of BD Pyxis MedStation 4000 AUX, REF 306 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-0974-2025
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 4000 AUX, REF 306

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 10885403512636, Serial Numbers: 9304700, 9305723, 9309302, 9413001, 9413014, 9415602, 9415665, 9417311, 9417312… UDI/DI 10885403512636, Serial Numbers: 9304700, 9305723, 9309302, 9413001, 9413014, 9415602, 9415665, 9417311, 9417312, 9417335, 9417340, 9417428, 9417430, 9417433, 9417437, 9418065, 9418068, 9418100, 9418105, 9418111, 9418112, 9418113, 9418114, 9418115, 9418129, 9418568, 9523679, 9525535, 9525558, 9525560, 9525561, 9525562, 9525582, 9525590, 9525600, 9525605, 9525606, 9525613, 9525624, 9525630, 9525638, 9525656, 9525657, 9526867, 9528530, 9528836, 9528859, 9528890, 9531253, 9531257, 12439518, 12439520, 12439521, 12439907, 12440208, 12440217, 12440218, 12440219, 12440220, 12440227, 12440339, 12440984, 12440985, 12443922, 12443923, 12445433, 12447385, 12447387, 12447388, 12447389, 12447394, 12447395, 12447396, 12448203, 12448204, 12452249, 12452265, 12452646, 12452649, 12453000, 12453215, 12453217, 12453238, 12453242, 12460386, 12460388, 12461366, 12461367, 12461927, 12462829, 12462831, 12462833, 12462835, 12463516, 12463517, 12463518, 12464145, 12464146, 12465451, 12465452, 12465453,

code_info

UDI/DI 10885403512636, Serial Numbers: 9304700, 9305723, 9309302, 9413001, 9413014, 9415602, 9415665, 9417311, 9417312…

UDI/DI 10885403512636, Serial Numbers: 9304700, 9305723, 9309302, 9413001, 9413014, 9415602, 9415665, 9417311, 9417312, 9417335, 9417340, 9417428, 9417430, 9417433, 9417437, 9418065, 9418068, 9418100, 9418105, 9418111, 9418112, 9418113, 9418114, 9418115, 9418129, 9418568, 9523679, 9525535, 9525558, 9525560, 9525561, 9525562, 9525582, 9525590, 9525600, 9525605, 9525606, 9525613, 9525624, 9525630, 9525638, 9525656, 9525657, 9526867, 9528530, 9528836, 9528859, 9528890, 9531253, 9531257, 12439518, 12439520, 12439521, 12439907, 12440208, 12440217, 12440218, 12440219, 12440220, 12440227, 12440339, 12440984, 12440985, 12443922, 12443923, 12445433, 12447385, 12447387, 12447388, 12447389, 12447394, 12447395, 12447396, 12448203, 12448204, 12452249, 12452265, 12452646, 12452649, 12453000, 12453215, 12453217, 12453238, 12453242, 12460386, 12460388, 12461366, 12461367, 12461927, 12462829, 12462831, 12462833, 12462835, 12463516, 12463517, 12463518, 12464145, 12464146, 12465451, 12465452, 12465453,

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-0974-2025%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.