QYXClass 2
Outpatient Cardiac Telemetry
FDA adverse event reports and recall history for outpatient cardiac telemetry (product code QYX), from the public MAUDE corpus and the live FDA recall database.
- Total reports
- 638
- Deaths
- 13
- Injuries
- 76
- Malfunctions
- 549
Reports per year
7423
40024
11025
5426
Source: FDA adverse event reports by year received, 2023–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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