Medical Device Recalls
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Related Medical Device Recalls |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Z-3013-2026 - 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. | 2 | 08/25/2026 |
FEI # 1523530 Midmark Corporation |
| Z-3012-2026 - Midmark IQecg Digital ECG, Model/Catalog Number: 4-000-0061, 4-000-0062 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18. | 2 | 08/25/2026 |
FEI # 1523530 Midmark Corporation |
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