Quick summary: Plum Solo and Plum Duo Precision IV Pumps. Reason: Performance. Category: General hospital and personal use. Date: 2026-05-14.
Plum Solo and Plum Duo Precision IV Pumps
2026-05-14
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.
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
Affected products
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
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
Frequently asked questions
Answers based on the official recall notice.
Product images
Official product images from Health Canada.
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