FDA Device recall Z-0975-2025

BD Pyxis Med ES Auxiliary (AUX), REF 343

FDA Device
Class II
ongoing
Published 2025-01-29

On 2025-01-29 the FDA classified a Class II recall of BD Pyxis Med ES Auxiliary (AUX), REF 343 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-0975-2025
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 Med ES Auxiliary (AUX), REF 343

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 10885403512698, Serial Numbers: 16171753, 16191650, 16192894, 16144435, 16154605, 16154606, 16154607, 16191713,… UDI/DI 10885403512698, Serial Numbers: 16171753, 16191650, 16192894, 16144435, 16154605, 16154606, 16154607, 16191713, 16191714, 16191715, 16191716, 16191718, 16191719, 16191720, 16191721, 16191722, 16196167, 16186595, 16196168, 16196169, 16186597, 16196170, 16196172, 16163310, 16179747, 16168959, 16167684, 16163677, 16185817, 16188363, 16188367, 16188695, 16185802, 16188322, 16191726, 16173525, 16173527, 16173528, 16194920, 16194922, 16190720, 16186580, 16191729, 16191730, 16191876, 16191877, 16191878, 16191879, 16166841, 16166842, 16182585, 16183929, 16178220, 16178222, 16179754, 16179750, 16179751, 16179752, 16179756, 16179757, 16179758, 16179759, 16179761, 16179762, 16184811, 16179764, 16179753, 16179765, 16179766, 16179767, 16179768, 16191682, 16191683, 16191684, 16188702, 16188705, 16172879, 16190710, 16190711, 16177195, 16177196, 16177199, 16177368, 16177369, 16191880, 16191881, 16188361, 16188364, 16188694, 16189315, 16173027, 16180723, 16173028, 16162674, 16186590, 16166843,

code_info

UDI/DI 10885403512698, Serial Numbers: 16171753, 16191650, 16192894, 16144435, 16154605, 16154606, 16154607, 16191713,…

UDI/DI 10885403512698, Serial Numbers: 16171753, 16191650, 16192894, 16144435, 16154605, 16154606, 16154607, 16191713, 16191714, 16191715, 16191716, 16191718, 16191719, 16191720, 16191721, 16191722, 16196167, 16186595, 16196168, 16196169, 16186597, 16196170, 16196172, 16163310, 16179747, 16168959, 16167684, 16163677, 16185817, 16188363, 16188367, 16188695, 16185802, 16188322, 16191726, 16173525, 16173527, 16173528, 16194920, 16194922, 16190720, 16186580, 16191729, 16191730, 16191876, 16191877, 16191878, 16191879, 16166841, 16166842, 16182585, 16183929, 16178220, 16178222, 16179754, 16179750, 16179751, 16179752, 16179756, 16179757, 16179758, 16179759, 16179761, 16179762, 16184811, 16179764, 16179753, 16179765, 16179766, 16179767, 16179768, 16191682, 16191683, 16191684, 16188702, 16188705, 16172879, 16190710, 16190711, 16177195, 16177196, 16177199, 16177368, 16177369, 16191880, 16191881, 16188361, 16188364, 16188694, 16189315, 16173027, 16180723, 16173028, 16162674, 16186590, 16166843,

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-0975-2025%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.