Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

BD Pyxis MedBank MedPass Software Recalled by CareFusion 303, Inc. Due to After dispensing a timed dose medication for a...

Date: August 18, 2023
Company: CareFusion 303, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact CareFusion 303, Inc. directly.

Affected Products

BD Pyxis MedBank MedPass Software, REF: 139088-01

Quantity: 37

Why Was This 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.

Where Was This Sold?

This product was distributed to 3 states: FL, KS, MI

Affected (3 states)Not affected

About CareFusion 303, Inc.

CareFusion 303, Inc. has 163 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report