RecallReported September 2, 2026
Class II recall by Midmark Corporation
Midmark Digital ECG HD+12, HD+15, Model/Catalog Number: 4-000-0080 Software Version: Midmark IQecg Plugin versions starting with v10 and pri…
FDA's enforcement report of September 2, 2026 lists a Class II recall by Midmark Corporation of Versailles, OH. Product: Midmark Digital ECG HD+12, HD+15, Model/Catalog Number: 4-000-0080 Software Version: Midmark IQecg Plugin versions starting with v10 and pri…. Status: Ongoing.
On the record
- Recalling firm
- Midmark Corporation
- Location
- Versailles, OH
- Classification
- Class II
- Status
- Ongoing
- Recall number
- Z-3013-2026
- Product type
- Devices
- Recall initiated
- 2026-07-20
- Reported by FDA
- 2026-09-02
The full record
An account shows the reason for the recall, where the product was distributed and the lots.
What a recall is
FDA classifies a recall by the hazard. Class I: a reasonable probability that the product will cause serious adverse health consequences or death. Class II: the product may cause temporary or medically reversible harm, or the probability of serious harm is remote. Class III: the product is not likely to cause adverse health consequences.
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From FDA enforcement reports. The record may have changed since it was read.
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