device recall
saveCareFusion 303, Inc. device recall (Cls I)
July 8, 2025updated 2mo ago
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BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions — Reason: Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume. — Status: Ongoing
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