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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
2022-06-16VAIVoluntary action indicatedInBios International, Inc.4
2022-06-16VAIVoluntary action indicatedInBios International, Inc.4
2018-08-23VAIVoluntary action indicatedInBios International, Inc.4
2018-08-23VAIVoluntary action indicatedInBios International, Inc.4
2015-05-15NAINo action indicatedInBios International, Inc.0
2015-05-15NAINo action indicatedInBios International, Inc.0
2013-04-22VAIVoluntary action indicatedInBios International, Inc.1
2013-04-22VAIVoluntary action indicatedInBios International, Inc.1
2012-05-04VAIVoluntary action indicatedInBios International, Inc.14
2012-05-04VAIVoluntary action indicatedInBios International, Inc.14
2010-08-27NAINo action indicatedInBios International, Inc.0
2010-08-27NAINo action indicatedInBios International, Inc.0