Public recall detail

Plum Solo and Plum Duo Precision IV Pumps

2026-05-14

medium
General hospital and personal use Performance
Quick summary

Quick summary: Plum Solo and Plum Duo Precision IV Pumps. Reason: Performance. Category: General hospital and personal use. Date: 2026-05-14.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Plum Solo and Plum Duo Precision IV Pumps. Reason: Performance. Category: General hospital and personal use. Date: 2026-05-14.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandICU Medical, Inc.
ProductPlum Solo and Plum Duo Precision IV Pumps
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82074

Affected products

LotLogiciel: V1.0.3
Model40001-04-01
Serial numberLogiciel: V1.0.3
LotLogiciel: V1.2.3
Model40002-04-03
Serial numberLogiciel: V1.2.3

Issue

Internal testing revealed that under certain conditions, the pump may not display a soft limit alert. LifeShield infusion safety software provides the option to define the maximum dose for the infusion, enable bolus delivery, and define hard and soft limits for the bolus. If the clinician programs a bolus delivery with a medication ruleset that has a maximum dose and bolus soft limits (either lower or upper) defined, and the programmed bolus violates a soft limit, the pump does not notify the clinician of the soft limit violation before confirming and starting delivery. In this scenario, the pump allows the clinician to confirm and start the bolus without displaying the bolus soft limit alert pop-up, and the dose soft limit icon does not appear on the confirmation screen. The pump does display the soft limit icon on the delivery screen once the bolus starts. Hard limits continue to function as expected.

What you should do

  • Please contact ICU Medical, device correction inquires, regaring this action: https://icumed.custhelp.com/app/marketaction
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - General hospital and personal use
CompaniesICU Medical, Inc. 600 North Field Drive, Lake Forest, Illinois, United States, 60045
Recall date2026-05-01
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82074
Background{}
CompaniesICU Medical, Inc. 600 North Field Drive, Lake Forest, Illinois, United States, 60045
AudiencesHealthcare
Source updated2026-05-14

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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