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Verathon Medical ULC

FDA adverse event reports naming Verathon Medical ULC as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: VERATHON MEDICAL ULC.

Total reports
2,803
Deaths
12
Injuries
35
Malfunctions
2,756

Reports per year

11
13
14
15
16
17
18
19
20
21
22
23
24
25
26

Source: FDA adverse event reports by year received, 20112026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.

Top device categories

Recent recalls

No recalls listed in the FDA device recall database for this entry.

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