Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BD Pyxis MedBank System - Product Label/labeling pending Recalled by CareFusion 303, Inc. Due to Due to customer complaints related to the MedBank...
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 System - Product Label/labeling pending
Quantity: 6,796 systems
Why Was This Recalled?
Due to customer complaints related to the MedBank software which may indicate that a different medication is loaded in a cubie (drawer) pocket than what is physically loaded and listed on the pocket label. As a result of this issue, a patient could receive the wrong medication or wrong dose of medication that could lead to patient harm.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CareFusion 303, Inc.
CareFusion 303, Inc. has 163 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report