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Medical Device

BD Alaris" System with Guardrails" Suite MX with Point of Care Unit

Recall date: 2026-04-01 · Source: FDA_DEVICE
Brand / Firm
CareFusion 303, Inc.
Product
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
Reason for recall
Due to product labeling not indicating which Transport Layer Security (TLS) version that must be enabled on hospital network to ensure secure Wi-Fi communication with Point-of-Care Units
Units affected
1,025,567
Description
BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
View official recall notice →