Z-2298-2026 Class II Ongoing

Recalled by CareFusion 303, Inc. — San Diego, CA

Recall Details

Product Type
Devices
Report Date
June 10, 2026
Initiation Date
April 30, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
15,933

Product Description

BD Pyxis MedStation ES REF: 323 Medication cabinet

Reason for Recall

Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

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

Code Information

All Serial Numbers/UDI:10885403512667