TemporaryFDAOngoing
Can cause harm that is usually temporary.
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
Check the device or its packaging for
Model No: 1-200-0320; UDI-DI: 00841709105791; Kit No: 4-000-0622; UDI-DI: 00841709105876; Kit Serial Number: V2900924; Zone Serial Number: V2899738
- Why
- A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
- Distributed
- US Nationwide distribution.
- Company
- Midmark Corporation
- Announced
- This is the date the recall was announced. A company may have started it weeks earlier.
- Recall began
Source: FDA record Z-3217-2026 · retrieved 18 September 2026
Read the official notice