Class IIOngoingZ-3220-2026
Midmark Corporation recalls Midmark IQvitals Zone
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Midmark CorporationOHSep 30, 2026
Midmark Corporation recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–6 of 6 recalls
Class IIOngoingZ-3219-2026
Midmark Corporation recalls Midmark IQvitals Zone
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Midmark CorporationOHSep 30, 2026
Class IIOngoingZ-3218-2026
Midmark Corporation recalls Midmark IQvitals Zone
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Midmark CorporationOHSep 30, 2026
Class IIOngoingZ-3217-2026
Midmark Corporation recalls Midmark IQvitals Zone
A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.
Midmark CorporationOHSep 30, 2026
Class IIOngoingZ-3013-2026
Midmark Corporation recalls Midmark Digital ECG HD+12
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.
Midmark CorporationOHSep 2, 2026
Class IIOngoingZ-3012-2026
Midmark Corporation recalls Midmark IQecg Digital ECG
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.
Midmark CorporationOHSep 2, 2026