Medical Device

Plum Duo Precision IV Pump, 40002-0403

Recall date: 2026-06-17 · Source: FDA_DEVICE

Brand / Firm

Product

Reason for recall

Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and starting delivery. This may potentially lead to under- or over-delivery.

Units affected

13,613

Description

Plum Duo Precision IV Pump, 40002-0403

View official recall notice →