FDA Device recall Z-0239-2026

BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409

FDA Device
Class II
ongoing
Published 2025-10-29

On 2025-10-29 the FDA classified a Class II recall of BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409 by Becton Dickinson And, citing product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials a….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0239-2026
Classification	Class II
Status	ongoing
Initiated	2025-09-23
Published	2025-10-29
Last updated	2026-09-13 11:57 UTC
Company	Becton Dickinson And
Distribution	US

Product

BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.

Reason

Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.

Identifiers

code_info	Catalog Number (Serial Numbers): 443624, UDI/DI: 00382904436247, (PF4176, PF4182, PF2302, PF4198, PF4149, PF4189, PF420… Catalog Number (Serial Numbers): 443624, UDI/DI: 00382904436247, (PF4176, PF4182, PF2302, PF4198, PF4149, PF4189, PF4202, PF2699, PF4200, PF4207, PF4209, PF2640, PF2769, PF3383, PF2742, PF4215, PF4204, PF0571, PF4188, PF4216, PF1642, PF4231, PF0929, PF4240, PF3443, PF0934, PF4232, PF4212, PF0566, PF3126, PF5436, PF5384, PF5396, PF5398, PF5404, PF3345, PF5443, PF3203, PF0598, PF3447, PF0601, PF5489, PF5495, PF5022, PF5063, PF3362, PF3340, PF5459, PF5492, PF5462, PF5499, PF0703, PF5466, PF0880, PF0705, PF5525, PF5469, PF5471, PF3397, PF4309, PF4397, PF5547, PF0632, PF0638, PF4443, PF0637, PF5200, PF5549, PF5202, PF5550, PF0643, PF5049, PF0639, PF3204, PF5207, PF5094, PF5209, PF5117, PF1352, PF5217, PF5148, PF5231, PF5195, PF5097, PF5162, PF5109, PF5169, PF5179, PF5183, PF2063, PF5197, PF5203, PF5168, PF5323, PF5329, PF0687, PF5352, PF5353, PF5418, PF5350, PF5359, PF5227, PF5351, PF5365, PF5218, PF5361, PF5389, PF5265, PF5266, PF5328, PF5337, PF0707, PF6126, PF0718, PF5356, PF5403, PF6167

code_info

Catalog Number (Serial Numbers): 443624, UDI/DI: 00382904436247, (PF4176, PF4182, PF2302, PF4198, PF4149, PF4189, PF420…

Catalog Number (Serial Numbers): 443624, UDI/DI: 00382904436247, (PF4176, PF4182, PF2302, PF4198, PF4149, PF4189, PF4202, PF2699, PF4200, PF4207, PF4209, PF2640, PF2769, PF3383, PF2742, PF4215, PF4204, PF0571, PF4188, PF4216, PF1642, PF4231, PF0929, PF4240, PF3443, PF0934, PF4232, PF4212, PF0566, PF3126, PF5436, PF5384, PF5396, PF5398, PF5404, PF3345, PF5443, PF3203, PF0598, PF3447, PF0601, PF5489, PF5495, PF5022, PF5063, PF3362, PF3340, PF5459, PF5492, PF5462, PF5499, PF0703, PF5466, PF0880, PF0705, PF5525, PF5469, PF5471, PF3397, PF4309, PF4397, PF5547, PF0632, PF0638, PF4443, PF0637, PF5200, PF5549, PF5202, PF5550, PF0643, PF5049, PF0639, PF3204, PF5207, PF5094, PF5209, PF5117, PF1352, PF5217, PF5148, PF5231, PF5195, PF5097, PF5162, PF5109, PF5169, PF5179, PF5183, PF2063, PF5197, PF5203, PF5168, PF5323, PF5329, PF0687, PF5352, PF5353, PF5418, PF5350, PF5359, PF5227, PF5351, PF5365, PF5218, PF5361, PF5389, PF5265, PF5266, PF5328, PF5337, PF0707, PF6126, PF0718, PF5356, PF5403, PF6167

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-0239-2026%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.