# FDA recall Z-3217-2026

> **Midmark Corporation** · Class II · device recall initiated 2026-08-21.

## Product

Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal), and oxygen saturation (SpO2) for adult and pediatric patients, Model Number: 1-200-0320 with Kit Number: 4-000-0622

## Reason for recall

A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-3217-2026
- **Recalling firm:** Midmark Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-08-21
- **Report date:** 2026-09-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Versailles, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3217-2026

## Citation

> MORVS. FDA recall Z-3217-2026. Retrieved 2026-10-20 from https://api.morvs.ai/recall/Z-3217-2026. Source: US FDA. Licensed CC0.

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