Skip to content
Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

No adverse-event reports are linked to this device.

Recall history

No recalls linked.

Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2022-04-08NAINo action indicatedVyaire Medical, Inc.0
2017-05-05NAINo action indicatedVyaire Medical, Inc.0
2016-05-11NAINo action indicatedVyaire Medical, Inc.0
2014-10-31VAIVoluntary action indicatedVyaire Medical, Inc.4
2014-10-08NAINo action indicatedVyaire Medical Inc0
2014-09-30NAINo action indicatedVyaire Medical0
2012-09-05VAIVoluntary action indicatedVyaire Medical5
2012-01-10NAINo action indicatedVyaire Medical0
2012-01-10NAINo action indicatedVyaire Medical0
2011-11-25NAINo action indicatedVyaire Medical0
2011-08-22NAINo action indicatedVyaire Medical, Inc.0
Similar devices
Select up to two to place side-by-side with this device.