Recalling firm
CareFusion 303, Inc.
Product type
Device
Status
Ongoing
Report date
2026-06-10
Distribution
US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW
Firm state
CA
Product quantity
709 units
Initiated by
Voluntary: Firm initiated
Reason for recall
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
Product description
BD Pyxis Mini Main REF: 349 Medication cabinet
Code / lot info
All Serial Numbers/UDI:10885403512582
Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.