Recall Atlas

Midmark recalls

2 official recalls and safety alerts involving Midmark since 2026-09, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Midmark or the relevant agency.

  1. 2026-09-30
  2. US
    Drugs & medicalClass II

    Midmark Corporation recalls Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate, temperature (temporal),…

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

    FDA · DeviceMidmark CorporationUS Nationwide distribution.Official notice →
  3. 2026-09-02
  4. US
    Drugs & medicalClass II

    Midmark Corporation recalls Midmark Digital ECG HD+12, HD+15, Model/Catalog Number: 4-000-0080 Software Version: Midmark IQecg Plugin versions starting with v10 and…

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

    FDA · DeviceMidmark CorporationWorldwide distribution - US Nationwide and the country of Canada.Official notice →