FDA-Device2024-08-14Class II
BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P, REF: 169-82 containing software version 3.9.1.9
CareFusion 303, Inc.
Hazard
Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
Sold states
US Nationwide distribution including in the states of AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NV, NY, OH, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV.
Affected count
11 units
Manufactured in
10020 Pacific Mesa Blvd, San Diego, CA, United States
Products
BD PYXIS MEDBANK TWR MN CR-10HH-2FH-P, REF: 169-82 containing software version 3.9.1.9
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2488-2024Don't want to check this manually?
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