PlainRecalls
FDA Devices Moderate Class II Ongoing

BD Pyxis MedBank MedPass Software, REF: 139088-01

Reported: October 4, 2023 Initiated: August 18, 2023 #Z-2646-2023

Product Description

BD Pyxis MedBank MedPass Software, REF: 139088-01

Reason for Recall

After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to duplicate medication administration.

Details

Recalling Firm
CareFusion 303, Inc.
Units Affected
37
Distribution
US: FL, MI, KS
Location
San Diego, CA

Frequently Asked Questions

What product was recalled?
BD Pyxis MedBank MedPass Software, REF: 139088-01. Recalled by CareFusion 303, Inc.. Units affected: 37.
Why was this product recalled?
After dispensing a timed dose medication for a patient, the automated dispensing cabinet software may continue to show the already dispensed medication dose is still available for dispense, which could lead to duplicate medication administration.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 4, 2023. Severity: Moderate. Recall number: Z-2646-2023.