Public recall detail

Novum IQ LVP

2025-05-14

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Recall Safety notice
Quick summary

Quick summary: Novum IQ LVP. Date: 2025-05-14.

Recommended action

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

Recall details

Quick summary: Novum IQ LVP. Date: 2025-05-14.

Official details

Affected product details

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

BrandBaxter Healthcare Corporation
ProductNovum IQ LVP
IssueMedical devices - Performance
Recall classType II
IdentificationRA-77454

Affected products

ProductNovum IQ LVP
LotAll lots.
Model40700BAX
Serial numberAll lots.
DescriptionNovum IQ LVP

Issue

Baxter Corporation is issuing an urgent medical device correction for the Novum IQ LVP due to the potential for underinfusion following use of the "standby mode" feature, or if the device is powered off with the set loaded for an extended period of time. Recall Start Date: April 29, 2025

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
CompaniesBaxter Healthcare Corporation 1 Baxter Parkway, Deerfield, Illinois, United States, 60015
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-77454
Background{}
CompaniesBaxter Healthcare Corporation 1 Baxter Parkway, Deerfield, Illinois, United States, 60015
AudiencesHealthcare
Source updated2025-05-14

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

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