Midmark Corporation
2
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-09-02 to 2026-09-02
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-09-02 | FDA Device | FDA Recall: Midmark Digital ECG HD+12, HD+15, Model/Catalog Number: 4-000-0080 Software Version: Midmark IQecg | Midmark Corporation | Class II | N/A |
| 2026-09-02 | FDA Device | FDA Recall: Midmark IQecg Digital ECG, Model/Catalog Number: 4-000-0061, 4-000-0062 Software Version: Midmark I | Midmark Corporation | Class II | N/A |