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
2026-03-06NAINo action indicatedPerma Pure LLC0
2020-01-03NAINo action indicatedPerma Pure LLC0
2016-01-21NAINo action indicatedPerma Pure LLC0
2013-07-09VAIVoluntary action indicatedPerma Pure LLC6
2011-09-19VAIVoluntary action indicatedPerma Pure LLC1
2011-03-18OAIOfficial action indicatedPerma Pure LLC6
2010-09-21WLWarning LetterPerma Pure LLC
2010-08-23OAIOfficial action indicatedPerma Pure LLC12
Similar devices
Select up to two to place side-by-side with this device.