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

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Severity split

Class I 4 31%Class II 9 69%Class III 0 0%

By year

Ongoing verathon recalls

2 active
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIGlideScope Core Monitor recalled by VerathonVerathonPotency & Assay42 states
DeviceCLASS IIGlideScope Core FHD recalled by VerathonVerathonPotency & Assay42 states

All verathon recalls, newest first

13 total

About 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.