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
2025-08-01NAINo action indicatedHill-Rom, Inc.0
2024-04-12NAINo action indicatedHill-Rom Inc0
2022-07-29VAIVoluntary action indicatedHill-Rom, Inc.3
2021-11-19VAIVoluntary action indicatedHill-Rom Inc2
2017-06-22VAIVoluntary action indicatedHill-Rom, Inc.2
2014-12-19VAIVoluntary action indicatedHill-Rom Inc2
2014-09-19NAINo action indicatedHill-Rom Company Inc.0
2014-05-06NAINo action indicatedHill-Rom, Inc.0
2014-02-13OAIOfficial action indicatedHill-Rom Inc8
2013-01-11OAIOfficial action indicatedHill-Rom Inc6
2012-03-02WLWarning LetterHill-Rom Inc
2011-10-11OAIOfficial action indicatedHill-Rom Inc0
2010-09-01NAINo action indicatedHill-Rom, Inc.0
2010-07-06VAIVoluntary action indicatedHill-Rom Inc2
Similar devices
Select up to two to place side-by-side with this device.