BD Pyxis MedStation ES Tower REF: 352 Medication cabinet recall (CareFusion 303, Inc.)
Medical deviceClass IIOngoing
Summary: CareFusion 303, Inc. is recalling BD Pyxis MedStation ES Tower REF: 352 Medication cabinet. Reason: Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
What is being recalled
BD Pyxis MedStation ES Tower REF: 352 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:10885403512674
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 number | Z-2302-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | April 30, 2026 |
| Reported | June 10, 2026 |
| Company | CareFusion 303, Inc. |
| Company location | San Diego, CA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 465 units |
More recalls from CareFusion 303, Inc. · all medical device recalls · recalls from April 2026