Midmark IQvitals Zone: recall status

⚠ Recalls found. Midmark IQvitals Zone is named in 4 official recalls in our current data:

FDA Class II recall Z-3217-2026 — A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
FDA Class II recall Z-3218-2026 — A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
FDA Class II recall Z-3219-2026 — A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
And 1 more listed below.

Recalls naming this model

FDA Class II · Medical device · September 30, 2026

A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

Company / brand: Midmark recalls

Official ID Z-3217-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

Company / brand: Midmark recalls

Official ID Z-3218-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

Company / brand: Midmark recalls

Official ID Z-3219-2026 · Official record ↗

FDA Class II · Medical device · September 30, 2026

A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

Company / brand: Midmark recalls

Official ID Z-3220-2026 · Official record ↗

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Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.