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Midmark Corporation recalls Midmark Digital ECG HD+12, HD+15, Model/Catalog Number: 4-000-0080 Software Version: Midmark IQecg Plugin versions star
Recalled September 2, 2026 · FDA recall Z-3013-2026 · Midmark
Hazard
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation. · FDA Class II
Units
3624 units
Sold at
Worldwide distribution - US Nationwide and the country of Canada.
Description
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.
Product
Midmark Digital ECG HD+12, HD+15, Model/Catalog Number: 4-000-0080 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18.
Manufacturer(s)
Midmark Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →