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
2023-12-05VAIVoluntary action indicatedNovum Medical Products of NY, LLC1
2021-07-13VAIVoluntary action indicatedNovum Medical Products of NY, LLC2
2018-07-13VAIVoluntary action indicatedNovum Medical Products of NY, LLC3
2014-11-06VAIVoluntary action indicatedNovum Medical Products of NY, LLC0
2013-11-15VAIVoluntary action indicatedNovum Medical Products of NY, LLC14
2012-01-13VAIVoluntary action indicatedNovum Medical Products of NY, LLC6
Similar devices
Select up to two to place side-by-side with this device.