FDA recall Z-2298-2026

CareFusion 303, Inc. · Class II · device

Product

BD Pyxis MedStation ES REF: 323 Medication cabinet

Reason for recall

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

Distribution

US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW

Key facts

Status
Ongoing
Initiation date
2026-04-30
Report date
2026-06-10
Voluntary/Mandated
Voluntary: Firm initiated
Location
San Diego, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2298-2026