BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology Sys
Pending LLM rewrite. Source: FDA_DEVICE Z-0239-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
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.
The recalled product
- Product
- BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
- Manufacturer
- Becton Dickinson & Co.
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- 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
Distribution
Distributed nationwide across the United States.
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