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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
2022-08-05NAINo action indicatedDiversatek Healthcare0
2022-08-05NAINo action indicatedDiversatek Healthcare0
2016-06-29NAINo action indicatedDiversatek Healthcare0
2016-06-29NAINo action indicatedDiversatek Healthcare0
2014-07-21VAIVoluntary action indicatedDiversatek Healthcare7
2014-07-21VAIVoluntary action indicatedDiversatek Healthcare7
2012-06-25VAIVoluntary action indicatedDiversatek Healthcare2
2012-06-25VAIVoluntary action indicatedDiversatek Healthcare2
2011-07-06VAIVoluntary action indicatedDiversatek Healthcare4
2011-07-06VAIVoluntary action indicatedDiversatek Healthcare4
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