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Baxter Healthcare Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS - safety alert

Official notice

20 Aug 2025

CriticalFDA

An official FDA notice concerns Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2025-08-20. Recall numbers: Z-2173-2025. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

36,705

Recall number

Z-2173-2025

Official notice

2025-08-20

The hazard

Health risk requiring medical assessment

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.

Event Ids

97164

Recall Numbers

Z-2173-2025

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Affected products

Product 1

Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS

Units affected

36,705

Risk / hazard

Health risk requiring medical assessment

Where it was sold

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

Location 1

US · United States

Affected area 1

US · United States

Affected area 2

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Baxter Healthcare. Contact: Baxter Healthcare Corporation.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class I

App estimate

critical

Recall details

Recall number

Z-2173-2025

Event id

97164

Units affected

36,705

Status

active

Classification

Class 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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