BD Phoenix M50 Instrument — Class II medical device recall Z-0239-2026
Ongoing recall by Becton Dickinson & Co., reported 2025-10-29, distributed nationwide. Product service credentials used by some BD technical support teams to access certain BD products were accesse
| Recall number | Z-0239-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Co., Sparks, MD, United States |
| Recall initiated | 2025-09-23 |
| Classified | 2025-10-23 |
| Reported by FDA | 2025-10-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BD, BE, BG, BH, BR, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DO, DZ, EC, EE, EG, ES, FI, FR, GB, GH, GR, GT, HK, HN, HR, HU, ID, IE, IL, IN, IQ, IR, IT, JO, JP, KE, KR, KW, LB, LK, LT, LU, MA, MT, MX, MY, NG, NL, NO, NP, NZ, OM, PA, PE, PH, PL, PT, PY, QA, RO, RS, RU, SA, SE, SG, SV, TH, TN, TR, TT, TW, UA, UY, VN, ZA |
| Quantity | 4,283 units |
| UPC / GTIN / UDI-DI | 00382904436247 |
| Serial numbers | 00382904436247, 443624, 44362409, PF0002, PF0004, PF0005, PF0006, PF0008, PF0011, PF0013, PF0015, PF0016, PF0017, PF0018, PF0019, PF0021, PF0022, PF0023, PF0024, PF0025, PF0028, PF0029, PF0032, PF0034, PF0035 and 475 more |
| Model numbers | 00382904436247, 443624, 44362409, PF0002, PF0004, PF0005, PF0006, PF0008, PF0011, PF0013, PF0015, PF0016, PF0017, PF0018, PF0019, PF0021, PF0022, PF0023, PF0024, PF0025, PF0028, PF0029, PF0032, PF0034, PF0035 and 475 more |
Product
BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology System, Catalog Numbers: 443624, 44362409.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0239-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.