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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
2025-07-10VAIVoluntary action indicatedFHC, Inc.2
2025-07-10VAIVoluntary action indicatedFHC, Inc.2
2024-11-26VAIVoluntary action indicatedFHC, Inc4
2024-11-26VAIVoluntary action indicatedFHC, Inc4
2019-07-24VAIVoluntary action indicatedFHC, Inc.3
2019-07-24VAIVoluntary action indicatedFHC, Inc.3
2015-10-29VAIVoluntary action indicatedFHC, Inc.5
2015-10-29VAIVoluntary action indicatedFHC, Inc.5
2012-02-10VAIVoluntary action indicatedFHC, Inc.10
2012-02-10VAIVoluntary action indicatedFHC, Inc.10
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