Class II — Midmark Corporation
| Recalling firm | MIDMARK CORP. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used. |
| 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: 1-200-0360 with Kit Number: 4-000-0724 |
| Quantity | 33 units |
| Distribution | US Nationwide distribution. |
| Initiated | 2026-08-21 |
| Classified | 2026-09-18 |
| Recall number | Z-3220-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Midmark Corporation (Z-3220-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99641/
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