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BD Pyxis MedStation ES REF: 323 Medication cabinet

Class II
Recalling firm
CareFusion 303, Inc.
Reason for recall
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Affected products (lot / model / serial)
All Serial Numbers/UDI:10885403512667
Units affected
15,933
Distribution pattern
US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
Firm location
San Diego, CA, United States
Recall type
Voluntary: Firm initiated
How the firm notified customers
Letter
Product type
Devices
Status
Ongoing
Recall number
Z-2298-2026
Recall initiated
April 30, 2026
FDA classification date
June 3, 2026
FDA report date
June 10, 2026
FDA event ID
98895
Last updated on HTM Vibe
July 23, 2026
View on openFDA