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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
2023-06-15VAIVoluntary action indicatedParks Medical Electronics, Inc4
2023-06-15VAIVoluntary action indicatedParks Medical Electronics, Inc4
2016-06-17VAIVoluntary action indicatedParks Medical Electronics, Inc4
2016-06-17VAIVoluntary action indicatedParks Medical Electronics, Inc4
2013-05-30VAIVoluntary action indicatedParks Medical Electronics, Inc2
2013-05-30VAIVoluntary action indicatedParks Medical Electronics, Inc2
2012-11-27WLWarning LetterParks Medical Electronics, Inc
2012-11-27WLWarning LetterParks Medical Electronics, Inc
2012-08-17OAIOfficial action indicatedParks Medical Electronics, Inc10
2012-08-17OAIOfficial action indicatedParks Medical Electronics, Inc10
2012-04-20VAIVoluntary action indicatedParks Medical Electronics, Inc8
2012-04-20VAIVoluntary action indicatedParks Medical Electronics, Inc8
2010-06-21VAIVoluntary action indicatedParks Medical Electronics, Inc3
2010-06-21VAIVoluntary action indicatedParks Medical Electronics, Inc3
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