Midmark recalls specific IQecg ECG models with outdated software that may show incorrect heart rate readings. Affected units include certain serial numbers and software versions. Update to v10.1.0.18 or later to fix.
A communication anomoly may result in incorrect electrocardiogram waveforms of a patient and an inaccurate beats-per-minute calculation.
Midmark is recalling specific IQecg Digital ECG devices that have software versions older than v10.1.0.18. This could cause incorrect heart rate readings and electrocardiogram waveforms, which might lead to misdiagnosis.
The software anomaly causes the device to display incorrect electrocardiogram waveforms and heart rate calculations. This could lead to misdiagnosis if healthcare providers rely on the device's readings without proper verification.
Healthcare professionals using Midmark IQecg ECG devices with software versions starting with v10 but before v10.1.0.18 are most at risk. Patients using these devices for heart monitoring could experience inaccurate readings.
Check if your device has a serial number starting with 480000 or 4820704. Software versions starting with v10 but before v10.1.0.18 are affected. The device may have lot codes 00841709100581, 00841709100321, 00841709100895, or 00841709100901.
Install software version v10.1.0.18 or later to correct the error.
Software versions starting with v10 but before v10.1.0.18 are affected.
Check your serial number (480000 or 4820704) and software version. Affected devices have lot codes 00841709100581, 00841709100321, 00841709100895, or 00841709100901.
No, but you must update the software to v10.1.0.18 or later to fix the issue.
We’ve drafted a message you can send Midmark to request your refund or repair — edit it as you like.
Subject: Recall Z-3012-2026 — Midmark Midmark Hello, I own a Midmark that is covered by recall Z-3012-2026 from Midmark. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
