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Midmark Corporation

Midmark Corporation: 2 recalls listed since August 2026 across FDA.

By year

  • 20262

By agency

  • FDA2

By category

  • Medical Device2

All recalls (2)

Midmark IQvitals Zone

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

Moderate riskFDADevice defect
Midmark IQvitals Zone

Midmark Digital ECG HD+12 and IQecg Digital ECG

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

Moderate riskFDADevice defect
Midmark Digital ECG HD+12 and IQecg Digital ECG