Verathon recalls
Verathon has 13 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 12 Jun 2024. 2 are still ongoing. The most frequent reason is device malfunction.
Total recalls13since 2012
Last 12 months0reported
Class I431% of total
Ongoing2latest 12 Jun 2024
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 4 31%Class II 9 69%Class III 0 0%
Why verathon is recalled
Product types
By year
Ongoing verathon recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | GlideScope Core Monitor recalled by Verathon | Verathon | Potency & Assay | 42 states |
| Device | CLASS II | GlideScope Core FHD recalled by Verathon | Verathon | Potency & Assay | 42 states |
All verathon recalls, newest first
13 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.