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

Class II

Recalling firm: Midmark Corporation
Reason for recall: A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Affected products (lot / model / serial): Model No: 1-200-0320; UDI-DI: 00841709105791; Kit No: 4-000-0622; UDI-DI: 00841709105876; Kit Serial Number: V2900924; Zone Serial Number: V2899738
Units affected: 1 units
Distribution pattern: US Nationwide distribution.
Firm location: Versailles, OH, United States
Recall type: Voluntary: Firm initiated
How the firm notified customers: Letter
Product type: Devices
Status: Ongoing
Recall number: Z-3217-2026
Recall initiated: August 21, 2026
FDA classification date: September 18, 2026
FDA report date: September 30, 2026
FDA event ID: 99641
Last updated on HTM Vibe: October 6, 2026