BD Pyxis MedStation ES — Class II medical device recall Z-1927-2024
Ongoing recall by CareFusion 303, Inc., reported 2024-06-05, distributed nationwide. Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
| Recall number | Z-1927-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | CareFusion 303, Inc., San Diego, CA, United States |
| Recall initiated | 2024-04-15 |
| Classified | 2024-05-30 |
| Reported by FDA | 2024-06-05 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AU, BE, BH, BM, BR, BS, CA, CL, CN, DE, ES, FI, FR, GB, GR, HK, IE, IT, JP, KR, KW, LB, MA, MX, NZ, OM, PT, QA, SG, TH, TW, ZA |
| Quantity | 212,367 units |
| UPC / GTIN / UDI-DI | 10885403512667 |
| Serial numbers | 0288, 049, 055, 071712, 08552, 110883, 115, 12330841, 12359549, 12375993, 12379349, 12385496, 12399496, 12399621, 12439897, 12440725, 12440974, 12440975, 12441103, 12441333, 12441335, 12441432, 12442985, 12443968, 12443969 and 475 more |
| Model numbers | 323 |
Product
BD Pyxis MedStation ES, REF: 323, Medication Cabinet
Reason for recall
Potential fluid ingress of anesthesia station or med station may result in smoke, system downtime and/or fire.
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-1927-2024. 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.