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
2025-02-24NAINo action indicatedFreudenberg Medical, LLC0
2025-02-24NAINo action indicatedFreudenberg Medical, LLC0
2022-03-01NAINo action indicatedFreudenberg Medical, LLC0
2022-03-01NAINo action indicatedFreudenberg Medical, LLC0
2016-09-19VAIVoluntary action indicatedFreudenberg Medical, LLC1
2016-09-19VAIVoluntary action indicatedFreudenberg Medical, LLC1
2016-07-22VAIVoluntary action indicatedFreudenberg Medical, LLC3
2016-07-22VAIVoluntary action indicatedFreudenberg Medical, LLC3
2015-07-22NAINo action indicatedFreudenberg Medical, LLC0
2015-07-22NAINo action indicatedFreudenberg Medical, LLC0
2013-06-21NAINo action indicatedFreudenberg Medical, LLC0
2013-06-21NAINo action indicatedFreudenberg Medical, LLC0
2013-01-18VAIVoluntary action indicatedFreudenberg Medical, LLC1
2013-01-18VAIVoluntary action indicatedFreudenberg Medical, LLC1
2012-03-27VAIVoluntary action indicatedFreudenberg Medical, LLC3
2012-03-27VAIVoluntary action indicatedFreudenberg Medical, LLC3
2011-11-18NAINo action indicatedFreudenberg Medical, LLC0
2011-11-18NAINo action indicatedFreudenberg Medical, LLC0
Similar devices
Select up to two to place side-by-side with this device.