Atlas FDA

Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to x.x

FDA device recall Z-1192-2023 · posted 2023-03-01 · Open, Classified

Recall details

Recalling firm
CareFusion 303, Inc.
Reason for recall
Infusion pump PCs with specific software/network cards/IP addresses can have network/wireless connection failure. Could cause inability to receive new datasets and inability to transfer retrospective analytics data to connected systems. Users with interfaces to electronic medication record or admin discharge transfer, may be unable to receive/send data; infusions may need to be manually programmed
Action taken
On 01/24/23, notices were mailed to customers, who were told to do the following: 1) Inspect the back of the PC Unit and observe the wireless card. Wireless cards that protrude out of the PC Unit are impacted. 2) Software version can be seen on the PCU using the following steps: a) Press Options Key, b) Press Page Down soft key, c) Press Software Versions soft key to display Software Versions menu, d) Press View soft key for the PCU. To prevent this issue from occurring, do one of the following: 1. Exclude IP address ranges ending in x.x.x.224 to x.x.x.255 from all the DHCP scopes where the affected PC Units are being utilized. 2. Assign the affected PC Units IP addresses utilizing DHCP reservations to prevent the PC Unit from obtaining an IP address in the aforementioned range. 3. Assign the affected PC Units a static IP address outside of the aforementioned range. Actions for Clinical Users: Check if wireless icon is illuminated. If the PC Unit is not connected to the wireless network when using Interoperability, the clinical user can input all infusion parameters manually. In addition, the clinical end user can manually document the infusion in the EMR. Data sets can also manually be programmed or uploaded to the PC unit using a serial cable. Continue to rely on hospital established protocols for wireless downtime procedures. Customers who require additional assistance can contact: Customer Order Management, 1-800-482-4822, GMB-CTS-CustCareInfusion@bd.com; Technical Support, 1-866-488-1408, DL-US-INF-TechSupport@bd.com; Clinical & Pharmacy Support, 1-858-617-1316, GMB-AlarisMedSafetyProgram@bd.com; BD Designated Complaint Handling Unit, 1-888-812-3266, productcomplaints@bd.com Complete and return the customer response form to BDRC39@bd.com
Root cause
Software Design Change
Status
Open, Classified
Product code
FRN
Quantity affected
83,185
Distribution
US: FL, CA, OR, IL, WI, NJ, AZ, NV, CO, WY, NE, TX, MI, VA, OH, NC, LA, NM, AL, TN, AR, PA, CT, IN, KS, GA, SC, MD, UT, MA, DC, OK, IA, NY, WA, SD, ND, MN, KY, MO, WV, MS, DE, ME, MT, ID, NH, HI, AK,
Date initiated
2023-01-24
Date posted
2023-03-01
Location
San Diego, CA

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RecordFirmDate
ALARIS SYSTEM WITH MMS, MODEL 8XXX (K072105)Cardinal Health 303,Inc.2007-12-28