Reported Sep 30, 2026 · Ongoing · Updated Oct 7, 2026
Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate,…
Midmark Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Midmark Corporation · 60 Vista Dr · Versailles, OH · 45380-9488
Is this the product you have?
- 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 Number1-200-0320
- with Kit Number4-000-0622
- Lot codes and dates
- Model No1-200-0320
- UDI-DI00841709105791
- Kit No4-000-0622
- UDI-DI00841709105876
- Kit Serial NumberV2900924
- Zone Serial NumberV2899738
- Amount recalled
- 1 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where 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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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