Midmark Corporation recalls
Every recall we track for Midmark Corporation — 6 in all, all from 2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
6 recalls since 2017.
All FDA recall records for Midmark Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 3 | 3 | 6 |
What to do if you have a recalled Midmark Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Midmark Corporation recalls
2 shown- Lower riskMedical device
Midmark Corporation recalls Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate,
Midmark recalls IQvitals Zone blood pressure monitors with model numbers 1-200-03300 and 1-200-0330 that may give inaccurate blood pressure readings when using the Linear Deflation Method. Affected units were sold between 2020 and 2023.
MidmarkAug 21, 2026 - Lower riskMedical device
Midmark Corporation recalls Midmark IQecg Digital ECG, Model/Catalog Number: 4-000-0061, 4-000-0062 Software Version: Midmark IQecg Plugin versions
Midmark recalls specific IQecg ECG models with outdated software that may show incorrect heart rate readings.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.
MidmarkJul 20, 2026
Midmark Corporation recall questions
How many recalls has Midmark Corporation had?
6 recalls from Midmark Corporation are on record with U.S. safety agencies, from 2026.
What is the most recent Midmark Corporation recall?
Midmark Corporation recalls Midmark IQvitals Zone, automatically and noninvasively measures systolic and diastolic blood pressure, pulse rate,, dated Aug 21, 2026. Every Midmark Corporation recall is listed on this page, newest first.
What should I do if I have a recalled Midmark Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Midmark Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.