Class II

Medical Device Recall: 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

Midmark Corporation · August 21, 2026

Reason for Recall

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

Product Description

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

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

1 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3217-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.