PlainRecalls
FDA Devices Moderate Class II Ongoing

BD Pyxis MedStation 4000 REF: 303. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.

Reported: February 19, 2025 Initiated: February 23, 2024 #Z-1125-2025

Product Description

BD Pyxis MedStation 4000 REF: 303. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.

Reason for Recall

Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.

Details

Recalling Firm
CareFusion 303, Inc.
Distribution
US: Nationwide OUS:JP IT IN DE GB KR NL TW ES BE AU BH CA BR NZ FR AR QA MX CL TR SA MY CH IL IE TH SG KW MA FI AE EG BS BM GR MC PL LB MO IQ TN NO PH CN HK CO JO OM
Location
San Diego, CA

Frequently Asked Questions

What product was recalled?
BD Pyxis MedStation 4000 REF: 303. Intended to securely store and dispense medications to a qualified and authorized healthcare provider.. Recalled by CareFusion 303, Inc..
Why was this product recalled?
Retroactive-Due to increase in complaints, their is a potential for drawer and/or door failures of the medication cabinet which could result in delay in accessing medications.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 19, 2025. Severity: Moderate. Recall number: Z-1125-2025.