Quick summary
Quick summary: Plum™ Precision IV Pumps. Reason: Health product recall. Category: Health products. Date: 2026-06-17.
Public recall detail
Plum™ Precision IV Pumps
2026-06-17
Health products
Health product recall
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™ Precision IV Pumps. Reason: Health product recall. Category: Health products. Date: 2026-06-17.
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™ Precision IV Pumps
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82218
Affected products
ProductPlum Solo™
Lotv1.0.3
Model40001-04-01
Serial numberv1.0.3
DescriptionPlum Solo™
ProductPlum Duo™
Lotv1.2.3
Model40002-04-03
Serial numberv1.2.3
DescriptionPlum Duo™
Issue
In a specific scenario, the pump will not decrement the Volume to be Infused (VTBI) displayed on the Delivery screen and may deliver up to twice the VTBI at the programmed rate.
What you should do
- Contact the manufacturer if you require additional information.
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 date2026-06-10
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82218
Background{}
CompaniesIcu Medical, Inc.600 North Field Drive, Lake Forest, Illinois, United States, 60045
AudiencesHealthcare
Source updated2026-06-17
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
FAQ
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Answers based on the official recall notice.
Product images
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