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Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal)

Official notice

30 Sept 2026

Last checked

6 Oct 2026

MediumFDA

An official FDA notice concerns Midmark. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2026-09-30. Recall numbers: Z-3219-2026. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

20

Recall number

Z-3219-2026

Official notice

2026-09-30

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.

Other

UDI-DI 00841709105821, UDI-DI 00841709105906

Event Ids

99641

Recall Numbers

Z-3219-2026

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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

Company & contacts

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Midmark. Contact: Midmark Corporation.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class II

App estimate

medium

Recall details

Recall number

Z-3219-2026

Event id

99641

Units affected

20

Status

active

Classification

Class II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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Brand match

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Markets

US

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