Midmark IQvitals Zone recall
Midmark Corporation recalled Midmark IQvitals Zone on September 30, 2026 because of a performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used. It was sold nationwide.
Why it was recalled
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
What's recalled
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: 1-200-0360 with Kit Number: 4-000-0724
Quantity: 33 units
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Midmark Corporation, Versailles, OH
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
US Nationwide distribution. - Status
- Ongoing
- Recall number
- Z-3220-2026
- Source
- U.S. Food and Drug Administration
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