Reported Oct 29, 2025 · Ongoing
BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers:…
Becton Dickinson & Co.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Becton Dickinson & Co. · 7 Loveton Cir · Sparks, MD · 21152-9212
Is this the product you have?
- BD Phoenix M50 Instrument
- labeled as the following1. BD Phoenix M50 Automated Microbiology System
- Catalog Numbers
44362444362409
- Lot codes and dates
- Catalog Number (Serial Numbers)443624
- UDI/DI
4,067 of 4,067 codes
00382904436247(PF4176PF4182PF2302PF4198PF4149PF4189PF4202PF2699PF4200PF4207PF4209PF2640PF2769PF3383PF2742PF4215PF4204PF0571PF4188PF4216PF1642PF4231PF0929PF4240PF3443PF0934PF4232PF4212PF0566PF3126PF5436PF5384PF5396PF5398PF5404PF3345PF5443PF3203PF0598PF3447PF0601PF5489PF5495PF5022PF5063PF3362PF3340PF5459PF5492PF5462PF5499PF0703PF5466PF0880PF0705PF5525PF5469PF5471PF3397
- Amount recalled
- 4,283 units
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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