medical MODERATE Updated 2026-06-17

ICU Medical, Inc. recalls Plum Duo Infusion Pump, 40002-0401

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Recalled Product

Plum Duo Infusion Pump, 40002-0401

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI M335400021 Plum Duo Infusion Pump v1.2.3

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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