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
2022-07-27NAINo action indicatedZimmer, Inc.0
2022-07-27NAINo action indicatedZimmer, Inc.0
2020-10-01NAINo action indicatedZimmer Manufacturing B.V.0
2017-10-16VAIVoluntary action indicatedZimmer, Inc.8
2017-10-16VAIVoluntary action indicatedZimmer, Inc.8
2017-09-01NAINo action indicatedZimmer Trabecular Metal Technology, Inc.0
2017-07-27VAIVoluntary action indicatedZIMMER ORTHOPEDIC MFG LTD3
2017-07-20VAIVoluntary action indicatedZimmer Manufacturing B.V.3
2016-05-27WLWarning LetterOrthosoft, Inc.
2016-05-23VAIVoluntary action indicatedZimmer Surgical Inc4
2015-11-20OAIOfficial action indicatedZimmer, Inc.10
2015-11-20OAIOfficial action indicatedZimmer, Inc.10
2015-11-17VAIVoluntary action indicatedZimmer Manufacturing B.V.4
2015-05-11VAIVoluntary action indicatedZimmer Trabecular Metal Technology, Inc.3
2014-10-16VAIVoluntary action indicatedZIMMER ORTHOPEDIC MFG LTD2
2014-06-11OAIOfficial action indicatedZimmer Manufacturing B.V.9
2014-05-28OAIOfficial action indicatedZimmer, Inc.12
2014-05-28OAIOfficial action indicatedZimmer, Inc.12
2014-02-07VAIVoluntary action indicatedZimmer, Inc.2
2014-02-07VAIVoluntary action indicatedZimmer, Inc.2
2013-08-19OAIOfficial action indicatedZimmer, Inc.0
2012-09-19WLWarning LetterZimmer Manufacturing B.V.
Similar devices
Select up to two to place side-by-side with this device.