FDA-Device2023-01-18Class II
BD Pyxis MedBank System - Product Label/labeling pending
CareFusion 303, Inc.
Hazard
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.
Sold states
U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, WA, WI, and WV.
Affected count
6,796 systems
Manufactured in
10020 Pacific Mesa Blvd, San Diego, CA, United States
Products
BD Pyxis MedBank System - Product Label/labeling pending
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0928-2023Don't want to check this manually?
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