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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
2025-01-13VAIVoluntary action indicatedArthrex, Inc.2
2025-01-13VAIVoluntary action indicatedArthrex, Inc.2
2023-05-05VAIVoluntary action indicatedArthrex, Inc.2
2023-05-05VAIVoluntary action indicatedArthrex, Inc.2
2016-08-25VAIVoluntary action indicatedArthrex, Inc.1
2016-08-25VAIVoluntary action indicatedArthrex, Inc.1
2013-09-27NAINo action indicatedArthrex Gmbh0
2013-09-27NAINo action indicatedArthrex Gmbh0
2013-09-25NAINo action indicatedARTHREX GMBH0
2013-09-25NAINo action indicatedARTHREX GMBH0
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