Recall Ledger

BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet recall (CareFusion 303, Inc.)

Medical deviceClass IIOngoing

Summary: CareFusion 303, Inc. is recalling BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet. Reason: Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

What is being recalled

BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet

Why

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

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

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

How to tell if yours is affected

All Serial Numbers/UDI:10885403517167

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-2303-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedApril 30, 2026
ReportedJune 10, 2026
CompanyCareFusion 303, Inc.
Company locationSan Diego, CA, United States
Initiated byVoluntary: Firm initiated
Quantity607 units

More recalls from CareFusion 303, Inc. · all medical device recalls · recalls from April 2026

Official FDA record