Midmark Corporation recalls Midmark IQvitals Zone
- Recalling company
- Midmark Corporation
- Product
- 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
- Reason
- A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 21, 2026
- Reported
- Sep 30, 2026
- Distribution
- US Nationwide distribution.
- Status
- Ongoing
- Quantity
- 1 units
- Lot / codes
- Model No: 1-200-0320; UDI-DI: 00841709105791; Kit No: 4-000-0622; UDI-DI: 00841709105876; Kit Serial Number: V2900924; Zone Serial Number: V2899738
- Company location
- Versailles, OH
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-3217-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-3217-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.