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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.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2025-10-16VAIVoluntary action indicatedGlobus Medical, Inc.1
2025-10-16VAIVoluntary action indicatedGlobus Medical, Inc.1
2025-08-13OAIOfficial action indicatedNevro Corporation6
2025-03-25NAINo action indicatedNuvasive Manufacturing LLC.0
2024-07-15WLWarning LetterGlobus Medical, Inc.
2024-07-15WLWarning LetterGlobus Medical, Inc.
2024-03-07OAIOfficial action indicatedGlobus Medical, Inc.6
2024-03-07OAIOfficial action indicatedGlobus Medical, Inc.6
2023-12-20VAIVoluntary action indicatedNevro Corporation1
2022-07-29NAINo action indicatedNevro Medical SRL0
2022-04-26NAINo action indicatedNevro Corporation0
2019-10-23NAINo action indicatedGlobus Medical, Inc.0
2019-10-23NAINo action indicatedGlobus Medical, Inc.0
2019-09-27VAIVoluntary action indicatedGlobus Medical, Inc.7
2019-09-27VAIVoluntary action indicatedGlobus Medical, Inc.7
2019-03-21NAINo action indicatedNevro Corporation0
2019-02-13VAIVoluntary action indicatedGlobus Medical, Inc.2
2019-02-13VAIVoluntary action indicatedGlobus Medical, Inc.2
2018-03-16NAINo action indicatedNevro Corporation0
2017-11-03VAIVoluntary action indicatedNevro Corporation5
2017-09-25NAINo action indicatedGlobus Medical, Inc.0
2017-09-25NAINo action indicatedGlobus Medical, Inc.0
2013-09-26WLWarning LetterGlobus Medical, Inc.
2013-09-26WLWarning LetterGlobus Medical, Inc.
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