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Novum iq large volume pump (lvp)

Official notice

9 Dec 2022

Last checked

9 Dec 2022

High riskHealth Canada

An official Health Canada notice concerns Novum iq large volume pump (lvp). Baxter Corporation is issuing an urgent medical device correction related to two different software issues that occur during use. The first issue observed is due to incorrect reported delivered volume while an infusion is running. The second issue observed is an unexpected screen transition during the 'air still detected' alarm workflow. Baxter Corporation is issuing a follow-up urgent medical device correction communication due to the Novum IQ Large Volume Infusion Pump (LVP) may not execute bolus initiations/ cancellations or titration adjustments as expected by the user. Recall start date: October 20, 2022 Published 2022-12-09.

What to do now

Contact the manufacturer if you require additional information.

Recall number

72081

Official notice

2022-12-09

The hazard

Baxter Corporation is issuing an urgent medical device correction related to two different software issues that occur during use. The first issue observed is due to incorrect reported delivered volume while an infusion is running. The second issue observed is an unexpected screen transition during the 'air still detected' alarm workflow. Baxter Corporation is issuing a follow-up urgent medical device correction communication due to the Novum IQ Large Volume Infusion Pump (LVP) may not execute bolus initiations/ cancellations or titration adjustments as expected by the user. Recall start date: October 20, 2022

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

72081

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Affected products

Product 1

Affected products - Novum Iq Large Volume Pump (LVP), Lot or serial number - All lots., Model or catalog number - 40700BAX

Risk / hazard

Baxter Corporation is issuing an urgent medical device correction related to two different software issues that occur during use. The first issue observed is due to incorrect reported delivered volume while an infusion is running. The second issue observed is an unexpected screen transition during the 'air still detected' alarm workflow. Baxter Corporation is issuing a follow-up urgent medical device correction communication due to the Novum IQ Large Volume Infusion Pump (LVP) may not execute bolus initiations/ cancellations or titration adjustments as expected by the user. Recall start date: October 20, 2022

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Baxter Healthcare, Novum Iq Large Volume Pump.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type I

App estimate

high

Recall details

Recall number

72081

Classification

Type I

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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