CareFusion 303, Inc. MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0, REF: 1139-00; MEDBANK TOWER MAIN, REF: 1145-00; MEDBANK MINI MAIN, REF: 1147-00 BD PYXIS MEDBANK Facility Software, REF: 139090-01; BD PYXS MEDBNK TWR MN 2HH1FH2HM2FM2FG1FF, REF: 169-100; BD PYXIS MEDBANK MINI 1HH-1FH- 1HM, REF: 169-101; BD PYXIS MEDBANK MINI 1HH-1HM- 1FM, REF: 169-102; BD PYXIS MEDBANK MINI 1HH-3HM, REF: 169-103; BD PYXIS MEDBANK MINI 2FH, REF: 169-104; BD PYXIS MEDBANK MINI 2FM, REF: 169-105; BD PYXIS MEDBANK MINI Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0, REF: 1139-00; MEDBANK TOWER MAIN, REF: 1145-00; MEDBANK MINI MAIN, REF: 1147-00 BD PYXIS MEDBANK Facility Software, REF: 139090-01; BD PYXS MEDBNK TWR MN 2HH1FH2HM2FM2FG1FF, REF: 169-100; BD PYXIS MEDBANK MINI 1HH-1FH- 1HM, REF: 169-101; BD PYXIS MEDBANK MINI 1HH-1HM- 1FM, REF: 169-102; BD PYXIS MEDBANK MINI 1HH-3HM, REF: 169-103; BD PYXIS MEDBANK MINI 2FH, REF: 169-104; BD PYXIS MEDBANK MINI 2FM, REF: 169-105; BD PYXIS MEDBANK MINI
Brand
CareFusion 303, Inc.
Lot Codes / Batch Numbers
BD Pyxis MedBank Receiving Cabinet Software Software versions: 2.1.2.11, 2.2.1.8, 2.31.8, 2.3.2.1, 2.4.2.26 REF/UDI-DI: 1119-00/10885403512704, 1137-00, 1139-00/10885403512704, 1145-00/10885403517167, 1147-00/10885403517181, 139090-01, 169-100/10885403512568, 169-101/10885403512544, 169-102/10885403512544, 169-103/10885403512544, 169-104/10885403512544, 169-105/10885403512544, 169-106/10885403512544, 169-107/10885403512544, 169-108/10885403512544, 169-109/10885403512544, 169-110/10885403512544, 169-111/10885403512544, 169-112/10885403512544, 169-113/10885403512544, 169-132/10885403512568, 169-137/10885403512544, 169-138/10885403512568, 169-139/10885403512568, 169-153/10885403512568, 169-155/10885403512568, 169-156/10885403512568, 169-159/10885403512544, 169-160/10885403512544, 169-161/10885403512544, 169-162/10885403512544, 169-23/10885403512568, 169-24/10885403512568, 169-25/10885403512568, 169-26/10885403512568, 169-27/10885403512568, 169-28/10885403512568, 169-29/10885403512568, 169-30/10885403512568, 169-31/10885403512568, 169-32/10885403512568, 169-33/10885403512568, 169-34/10885403512568, 169-35/10885403512568, 169-36/10885403512568, 169-37/10885403512568, 169-38/10885403512568, 169-39/10885403512568, 169-40/10885403512568, 169-41/10885403512568, 169-42/10885403512568, 169-43/10885403512568, 169-44/10885403512568, 169-45/10885403512568, 169-46/10885403512568, 169-47/10885403512568, 169-48/10885403512568, 169-49/10885403512568, 169-50/10885403512568, 169-51/10885403512568, 169-52/10885403512568, 169-53/10885403512568, 169-54/10885403512568, 169-55/10885403512568, 169-56/10885403512568, 169-57/10885403512568, 169-58/10885403512568, 169-59/10885403512568, 169-60/10885403512568, 169-61/10885403512568, 169-62/10885403512568, 169-63/10885403512568, 169-64/10885403512568, 169-65/10885403512568, 169-66/10885403512568, 169-67/10885403512568, 169-68/10885403512568, 169-69/10885403512568, 169-70/10885403512568, 169-71/10885403512568, 169-72/10885403512568, 169-73/10885403512568, 169-74/10885403512568, 169-75/10885403512568, 169-76/10885403512568, 169-77/10885403512568, 169-78/10885403512568, 169-79/10885403512568, 169-80/10885403512568, 169-81/10885403512568, 139089-01
Products Sold
BD Pyxis MedBank Receiving Cabinet Software Software versions: 2.1.2.11, 2.2.1.8, 2.31.8, 2.3.2.1, 2.4.2.26 REF/UDI-DI: 1119-00/10885403512704; 1137-00; 1139-00/10885403512704; 1145-00/10885403517167; 1147-00/10885403517181; 139090-01; 169-100/10885403512568; 169-101/10885403512544; 169-102/10885403512544; 169-103/10885403512544; 169-104/10885403512544; 169-105/10885403512544; 169-106/10885403512544; 169-107/10885403512544; 169-108/10885403512544; 169-109/10885403512544; 169-110/10885403512544; 169-111/10885403512544; 169-112/10885403512544; 169-113/10885403512544; 169-132/10885403512568; 169-137/10885403512544; 169-138/10885403512568; 169-139/10885403512568; 169-153/10885403512568; 169-155/10885403512568; 169-156/10885403512568; 169-159/10885403512544; 169-160/10885403512544; 169-161/10885403512544; 169-162/10885403512544; 169-23/10885403512568; 169-24/10885403512568; 169-25/10885403512568; 169-26/10885403512568; 169-27/10885403512568; 169-28/10885403512568; 169-29/10885403512568; 169-30/10885403512568; 169-31/10885403512568; 169-32/10885403512568; 169-33/10885403512568; 169-34/10885403512568; 169-35/10885403512568; 169-36/10885403512568; 169-37/10885403512568; 169-38/10885403512568; 169-39/10885403512568; 169-40/10885403512568; 169-41/10885403512568; 169-42/10885403512568; 169-43/10885403512568; 169-44/10885403512568; 169-45/10885403512568; 169-46/10885403512568; 169-47/10885403512568; 169-48/10885403512568; 169-49/10885403512568; 169-50/10885403512568; 169-51/10885403512568; 169-52/10885403512568; 169-53/10885403512568; 169-54/10885403512568; 169-55/10885403512568; 169-56/10885403512568; 169-57/10885403512568; 169-58/10885403512568; 169-59/10885403512568; 169-60/10885403512568; 169-61/10885403512568; 169-62/10885403512568; 169-63/10885403512568; 169-64/10885403512568; 169-65/10885403512568; 169-66/10885403512568; 169-67/10885403512568; 169-68/10885403512568; 169-69/10885403512568; 169-70/10885403512568; 169-71/10885403512568; 169-72/10885403512568; 169-73/10885403512568; 169-74/10885403512568; 169-75/10885403512568; 169-76/10885403512568; 169-77/10885403512568; 169-78/10885403512568; 169-79/10885403512568; 169-80/10885403512568; 169-81/10885403512568; 139089-01
CareFusion 303, Inc. is recalling MEDFLEX, REF: 1119-00; MEDBANK MAIN, REF: 1137-00; MEDFLEX 2.0, REF: 1139-00; MEDBANK TOWER MAIN, RE due to If "Clear All" selected medications is selected on patient profile, the automated dispensing cabinet may allow dispensing of medication without first . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
If "Clear All" selected medications is selected on patient profile, the automated dispensing cabinet may allow dispensing of medication without first requiring the RxVerify Validation Code be entered/without validation from a pharmacist, which could lead to unintended and incorrect medication removal.
Recommended Action
Per FDA guidance
05OCT2023, Customer Release Notes were sent to customers informing them of system release v1.3.4. On 2/18/2025, correction notices were mailed and emailed to Customers, Directors of Pharmacy, and Facility Medication Management Administrators who were informed the following: 1) Customers with system administrator privileges can uncheck the option for the "Clear All" button in the BD Pyxis MedBank Facility Software, which will disable the feature and prevent the button from displaying on the patient profile selection screen. 2) Best practice is to verify the item being removed is accurate against the provider s order, and if available utilize barcode medication administration as an additional check to ensure the correct medication is retrieved prior to administration.1 3) Share and disseminate this notice within your facility network to ensure they are aware of the field action. 4) Complete and return the Customer Response Form via email to BDRC23@bd.com BD Pyxis MedBank Facility Software version 2.5.1.4 within MedBank system release v1.7 is currently available and will address this issue. BD will contact impacted customers to schedule a time for software upgrade. If you have questions contact the firm's Technical Support at 1-866-930-9251 Phone Hours: 24 hours, 7 days a week.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026