Recall Z-0928-2023— CareFusion 303, Inc.
Class II · Ongoing
Class II FDA medical device recall by CareFusion 303, Inc., initiated 2022-12-12. FDA's recall record names no specific 510(k) clearance for this event. Product: BD Pyxis MedBank System - Product Label/labeling pending. Reason: 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..
- Recalling firm
- CareFusion 303, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-12-12
- Firm location
- San Diego, CA, United States
Product description
BD Pyxis MedBank System - Product Label/labeling pending
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.