أجهزة طبية
IQecg® Digital ECG
Summary
| Type | Health product recall |
|---|---|
| Product | IQecg® Digital ECG |
| Issue | Medical devices - Performance |
| What to do | Contact the manufacturer if you require additional information. |
| Audience | Healthcare |
| Brand(s) | Midmark Corporation |
| Last updated | 2026-10-19 |
Affected products
Affected products |
Lot or serial number |
Model or catalogue number |
|---|---|---|
IQecg® Digital ECG |
SW prior to v10.1.0.18 |
4-000-0061 |
IQecg® Digital ECG |
SW prior to v10.1.0.18 |
4-000-0062 |
IQecg® - Serial Version |
SW prior to v10.1.0.18 |
4-000-0060 |
Issue
Affected IQecg® plugin software may produce incorrect ECG waveforms and inaccurate heart-rate calculations. Until corrected software is installed, users should manually assess the patient's heart rate before initiating therapeutic intervention and use the temporary workaround if the issue occurs. Midmark will coordinate installation of the corrected software.
Details
| Original published date | 2026-07-28 |
|---|---|
| Alert / recall type | Health product recall |
| Category | Health products - Medical devices - Cardiovascular |
| Companies | Midmark Corporation 60 Vista Drive, Versailles, Ohio, United States, 45380 |
| Published by | Health Canada |
| Audience | Healthcare |
| Recall class | Type II |
| Recall date | 2026-10-15 |
| Identification number | RA-82412 |
Source: Government of Canada, Recalls and safety alerts – https://recalls-rappels.canada.ca/en/alert-recall/iqecgr-digital-ecg