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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
2024-06-14VAIVoluntary action indicatedPioneer Surgical Technology Inc.2
2024-06-14VAIVoluntary action indicatedPioneer Surgical Technology Inc.2
2023-05-11NAINo action indicatedPioneer Surgical Technology Inc.0
2023-05-11NAINo action indicatedPioneer Surgical Technology Inc.0
2017-03-28VAIVoluntary action indicatedPioneer Surgical Technology Inc.7
2017-03-28VAIVoluntary action indicatedPioneer Surgical Technology Inc.7
2016-06-23VAIVoluntary action indicatedPioneer Surgical Technology Inc.1
2016-06-23VAIVoluntary action indicatedPioneer Surgical Technology Inc.1
2014-07-11VAIVoluntary action indicatedPioneer Surgical Technology Inc.1
2014-07-11VAIVoluntary action indicatedPioneer Surgical Technology Inc.1
2012-03-28NAINo action indicatedPioneer Surgical Technology Inc.0
2012-03-28NAINo action indicatedPioneer Surgical Technology Inc.0
2010-12-21VAIVoluntary action indicatedPioneer Surgical Technology Inc.6
2010-12-21VAIVoluntary action indicatedPioneer Surgical Technology Inc.6
2010-08-03WLWarning LetterPioneer Surgical Technology Inc.
2010-08-03WLWarning LetterPioneer Surgical Technology Inc.
2010-04-22OAIOfficial action indicatedPioneer Surgical Technology Inc.10
2010-04-22OAIOfficial action indicatedPioneer Surgical Technology Inc.10
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