BD Pyxis MedBank (CareFusion) – restocking software issue (2025)
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 169-101; MINI 1HH-1HM-1FM, 169-102; MINI 2FH, 138902-01; MINI 2FH, 169-104; MINI 2FM, 169-105; MINI 2HH-1FH, 169-106; MINI 2HH-1FH, 138908-01; MINI 2HH-1FM, 169-107; MINI 2HH-1FM, 138906-01; MINI 3HH-1FG, 169-110; MINI 3HH-1FG, 139091-01; MINI 3HH-1HM, 169-111; MINI 4HH, 138910-01; MINI 4HH, 169-112; MINI 4HM, 169-113; MINI 4HM, 138915-01; TWR MN 10HH-1FH-1FM, 169-23; TWR MN 10HH-2FH, 169-24; TWR MN
Brand
CareFusion 303, Inc.
Lot Codes / Batch Numbers
REF/UDI-DI(GTIN)/Software Version: 139088-01/1.2.3.23, 169-137/10885403512544/2.4, 169-101/10885403512544/2.4, 169-102/10885403512544/2.4, 138902-01/2.4, 169-104/10885403512544/2.4, 169-105/10885403512544/2.4, 169-106/10885403512544/2.4, 138908-01/2.4, 169-107/10885403512544/2.4, 138906-01/2.4, 169-108/10885403512544/2.4, 169-110/10885403512544/2.4, 139091-01/2.4, 169-111/10885403512544/2.4, 138910-01/2.4, 169-112/10885403512544/2.4, 169-113/10885403512544/2.4, 138915-01/2.4, 169-23/10885403512568/2.4, 169-24/10885403512568/2.4, 138955-01/2.4, 169-25/10885403512568/2.4, 138924-01/2.4, 169-26/10885403512568/2.4, 138960-01/2.4, 169-27/10885403512568/2.4, 138961-01/2.4, 169-28/10885403512568/2.4, 138926-01/2.4, 138927-01/2.4, 169-29/10885403512568/2.4, 169-30/10885403512568/2.4, 169-31/10885403512568/2.4, 169-32/10885403512568/2.4, 169-33/10885403512568/2.4, 169-34/10885403512568/2.4, 169-139/10885403512568/2.4, 139125-01/2.4, 169-38/10885403512568/2.4, 138919-01/2.4, 169-39/10885403512568/2.4, 169-40/10885403512568/2.4, 169-41/10885403512568/2.4, 169-42/10885403512568/2.4, 138933-01/2.4, 169-140/10885403512568/1.2.3.23, 169-43/10885403512568/2.4, 169-44/10885403512568/2.4, 138959-01/2.4, 169-45/10885403512568/2.4, 169-46/10885403512568/2.4, 169-47/10885403512568/2.4, 169-49/10885403512568/2.4, 169-50/10885403512568/2.4, 138931-01/2.4, 169-52/10885403512568/2.4, 169-53/10885403512568/2.4, 138940-01/2.4, 169-54/10885403512568/2.4, 138952-01/2.4, 169-55/10885403512568/2.4, 169-56/10885403512568/2.4, 138918-01/2.4, 169-57/10885403512568/2.4, 169-59/10885403512568/2.4, 169-60/10885403512568/2.4, 138914-01/2.4, 169-61/10885403512568/2.4, 169-62/10885403512568/2.4, 169-63/10885403512568/2.4, 169-64/10885403512568/2.4, 169-65/10885403512568/2.4, 169-67/10885403512568/2.4, 138957-01/2.4, 169-68/10885403512568/2.4, 138922-01/2.4, 169-69/10885403512568/2.4, 169-71/10885403512568/2.4, 138958-01/2.4, 169-72/10885403512568/2.4, 138920-01/2.4, 169-73/10885403512568/2.4, 138937-01/2.4, 139086-01/2.4, 169-74/10885403512568/2.4, 169-75/10885403512568/2.4, 169-77/10885403512568/2.4, 169-78/10885403512568/2.4, 138939-01/2.4, 169-79/10885403512568/2.4, 169-80/10885403512568/2.4, 138956-01/2.4, 169-81/10885403512568/2.4, 138923-01/2.4, 139055-01/2.4, 139041-01/2.4, 139046-01/2.4, 139049-01/2.4, 139051-01/2.4, 139052-01/2.4, 139165-01/2.4, 139069-01/2.4, 1137-00/2.4, 1147-00/10885403517181/2.4, 1145-00/10885403517167/2.4, 1119-00/10885403512704/2.4, 1139-00/10885403512704/2.4
Products Sold
REF/UDI-DI(GTIN)/Software Version: 139088-01/1.2.3.23; 169-137/10885403512544/2.4; 169-101/10885403512544/2.4; 169-102/10885403512544/2.4; 138902-01/2.4; 169-104/10885403512544/2.4; 169-105/10885403512544/2.4; 169-106/10885403512544/2.4; 138908-01/2.4; 169-107/10885403512544/2.4; 138906-01/2.4; 169-108/10885403512544/2.4; 169-110/10885403512544/2.4; 139091-01/2.4; 169-111/10885403512544/2.4; 138910-01/2.4; 169-112/10885403512544/2.4; 169-113/10885403512544/2.4; 138915-01/2.4; 169-23/10885403512568/2.4; 169-24/10885403512568/2.4; 138955-01/2.4; 169-25/10885403512568/2.4; 138924-01/2.4; 169-26/10885403512568/2.4; 138960-01/2.4; 169-27/10885403512568/2.4; 138961-01/2.4; 169-28/10885403512568/2.4; 138926-01/2.4; 138927-01/2.4; 169-29/10885403512568/2.4; 169-30/10885403512568/2.4; 169-31/10885403512568/2.4; 169-32/10885403512568/2.4; 169-33/10885403512568/2.4; 169-34/10885403512568/2.4; 169-139/10885403512568/2.4; 139125-01/2.4; 169-38/10885403512568/2.4; 138919-01/2.4; 169-39/10885403512568/2.4; 169-40/10885403512568/2.4; 169-41/10885403512568/2.4; 169-42/10885403512568/2.4; 138933-01/2.4; 169-140/10885403512568/1.2.3.23; 169-43/10885403512568/2.4; 169-44/10885403512568/2.4; 138959-01/2.4; 169-45/10885403512568/2.4; 169-46/10885403512568/2.4; 169-47/10885403512568/2.4; 169-49/10885403512568/2.4; 169-50/10885403512568/2.4; 138931-01/2.4; 169-52/10885403512568/2.4; 169-53/10885403512568/2.4; 138940-01/2.4; 169-54/10885403512568/2.4; 138952-01/2.4; 169-55/10885403512568/2.4; 169-56/10885403512568/2.4; 138918-01/2.4; 169-57/10885403512568/2.4; 169-59/10885403512568/2.4; 169-60/10885403512568/2.4; 138914-01/2.4; 169-61/10885403512568/2.4; 169-62/10885403512568/2.4; 169-63/10885403512568/2.4; 169-64/10885403512568/2.4; 169-65/10885403512568/2.4; 169-67/10885403512568/2.4; 138957-01/2.4; 169-68/10885403512568/2.4; 138922-01/2.4; 169-69/10885403512568/2.4; 169-71/10885403512568/2.4; 138958-01/2.4; 169-72/10885403512568/2.4; 138920-01/2.4; 169-73/10885403512568/2.4; 138937-01/2.4; 139086-01/2.4; 169-74/10885403512568/2.4; 169-75/10885403512568/2.4; 169-77/10885403512568/2.4; 169-78/10885403512568/2.4; 138939-01/2.4; 169-79/10885403512568/2.4; 169-80/10885403512568/2.4; 138956-01/2.4; 169-81/10885403512568/2.4; 138923-01/2.4; 139055-01/2.4; 139041-01/2.4; 139046-01/2.4; 139049-01/2.4; 139051-01/2.4; 139052-01/2.4; 139165-01/2.4; 139069-01/2.4; 1137-00/2.4; 1147-00/10885403517181/2.4; 1145-00/10885403517167/2.4; 1119-00/10885403512704/2.4; 1139-00/10885403512704/2.4
CareFusion 303, Inc. is recalling BD PYXIS MEDBANK (Name, REF): MEDPASS MODULE, 139088-01; MINI 1FH-1FM, 169-137; MINI 1HH-1FH-1HM, 16 due to Users trying to restock a single bin location of an automated dispensing cabinet, during pocket exchange restocking workflow, may experience a softwar. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Users trying to restock a single bin location of an automated dispensing cabinet, during pocket exchange restocking workflow, may experience a software issue that results in 2 destock transactions and 2 stock transactions, which results in doubling the bin quantity, which may result in a delay in access to desired medications and/or supplies, which may lead to temporary body function impairment.
Recommended Action
Per FDA guidance
On 3/11/2025, correction notices were mailed and emailed to Medical Director, Risk Manager, Medical Device Safety Officer, Lab Manager, Clinical Engineering, and other customers asking them to take the following actions: 1) Best practice is to verify the total dose being removed is accurate against the provider's order, and if available utilize barcode medication administration as an additional check to ensure the correct dose is retrieved prior to administration. 2) Customers can inventory the CUBIE pocket via a cycle count or blind count to correct the inventory when discrepancies occur. Customers can refer to the BD Pyxis MedBank Cabinet User Guide - 10000414987 Ver. 01, Version v2.4 for instructions. Refer to chapter six (6), page 103. 3)Customers should ensure backup procedures (which may include but are not limited to keys, emergency medication supplies, alternate devices in proximity, etc) are in place and staff have all been properly educated on them. 4) Share this letter with any facilities within your network that you may have distributed affected devices to. 5) Post this Recall Letter on or near affected products as a reminder of the recall and the steps/instructions that are needed to be followed. 6) Complete and return the Response Form via email to bdrc44@bd.com Firm is in the process of contacting all customers to schedule an appropriate time for the software upgrade to MedBank software version 1.7. If you require further assistance contact the firm's Technical support: 1-866-930-9251 Phone Hours: 24 hours, 7 days a week Website: https://bdx.my.site.com/CC360/s/impactedproducts?rn=MMS-24-5163/MMS-25-5183/5184
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