Source: MassDevice

Verathon: FDA: Verathon recall of video laryngoscope is Class I

The FDA today labeled a recall notice from Verathon for its GlideScope Titanium single-use video laryngoscope due to issues with potential video feed disruption. Class I recall designations, the agency's most serious classification of recall, are used when there is a reasonable probability that product use could cause serious adverse health consequences or death. The [...]The post FDA: Verathon recall of video laryngoscope is Class I appeared first on MassDevice.

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Earl Thompson's photo - President of Verathon

President

Earl Thompson

CEO Approval Rating

87/100

Verathon designs, manufactures and markets medical devices such as video laryngoscopy and bladder volume measurement. Read more