FDA Adverse Event
Malfunction
Summary report: N
BD PYXIS¿ MEDSTATION¿ ES
MDR report key: 24910336
·
Received April 17, 2026
Report
- Report Number
- 2016493-2026-22254
- Event Type
- Malfunction
- Date Received
- April 17, 2026
- Date of Event
- March 20, 2026
- Report Date
- April 20, 2026
- Manufacturer
- CAREFUSION 303, INC.
- Product Code
- BRY
- UDI-DI
- 10885403533228
- PMA / PMN Number
- EXEMPT
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
Additional Manufacturer Narrative · 0
A DEVICE EVALUATION IS ANTICIPATED BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.
Description of Event or Problem · 0
IT WAS REPORTED THAT WHEN USING THE BD PYXIS¿ MEDSTATION¿ ES ENTIRE MEDICATION DRAWER FELL OUT OF THE RAIL AND BROKE. THE DRAWER COULD NOT BE CLOSED BECAUSE THE RAIL WAS BROKEN. THE CUSTOMER STATED THAT THERE WAS A DELAY IN PATIENT CARE. THERE WERE NO ADVERSE EVENTS OR INJURIES REPORTED BASED ON THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 434220 | BD PYXIS¿ MEDSTATION¿ ES | AUTOMATED DISPENSING CABINET | BRY | CAREFUSION 303, INC. | 500001002500 | 10885403533228 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |