Recall of BD Alaris Pump Module model 8100 with specific UDI-DI codes due to potential connectivity problems with hospital networks caused by daylight savings time adjustments.
Due to a number of modules flashed with a date and time associated with the daylight savings time (DST) adjustment that may cause connectivity issue with hospital networks. This issue only affects the Interoperability workflow for devices with a DST invalid timestamp, impacting connectivity of the PCU to the hospital network
BD Alaris Pump Module model 8100 units with specific UDI-DI codes were recalled because they may have connectivity issues with hospital networks due to incorrect daylight savings time settings. This could affect the system's ability to communicate with hospital networks during certain workflows.
The pump modules were flashed with a date and time associated with daylight savings time adjustments that could cause invalid timestamps. This may lead to connectivity problems with hospital networks specifically for the Interoperability workflow, affecting how the pump communicates with the hospital's system.
Healthcare facilities using BD Alaris Pump Module model 8100 with the listed UDI-DI codes are most at risk. Patients receiving fluid administration through this system may be affected if the connectivity issue impacts treatment workflows.
Check for the UDI-DI code 10885403810046 on the pump module. The affected units are part of the BD Alaris System with Guardrails Suite MX and have specific serial numbers listed in the recall notice.
Verify the UDI-DI code and serial numbers listed in the recall notice to confirm if your pump module is affected.
The pump modules may have connectivity issues with hospital networks due to incorrect daylight savings time settings, which could affect the Interoperability workflow.
No, the recall does not require immediate discontinuation. Affected units may continue to be used but should be checked for connectivity issues.
Check for the UDI-DI code 10885403810046 and the specific serial numbers listed in the recall notice.
We’ve drafted a message you can send BD Alaris to request your refund or repair — edit it as you like.
Subject: Recall Z-1217-2026 — BD Alaris BD Alaris Hello, I own a BD Alaris that is covered by recall Z-1217-2026 from BD Alaris. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
