Midmark recalls

6 recent recalls on record for Midmark in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

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.

Official ID Z-3220-2026 · 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.

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.

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.

Official ID Z-3217-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.

Official ID Z-3013-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.

Official ID Z-3012-2026 · Official record ↗

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