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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
2018-09-26NAINo action indicatedPeregrine Surgical Ltd0
2018-09-26NAINo action indicatedPeregrine Surgical Ltd0
2015-06-19VAIVoluntary action indicatedPeregrine Surgical Ltd0
2015-06-19VAIVoluntary action indicatedPeregrine Surgical Ltd0
2013-02-07VAIVoluntary action indicatedPeregrine Surgical Ltd1
2013-02-07VAIVoluntary action indicatedPeregrine Surgical Ltd1
2011-06-30VAIVoluntary action indicatedPeregrine Surgical Ltd0
2011-06-30VAIVoluntary action indicatedPeregrine Surgical Ltd0
2010-12-20WLWarning LetterPeregrine Surgical Ltd—
2010-12-20WLWarning LetterPeregrine Surgical Ltd—
2010-07-15OAIOfficial action indicatedPeregrine Surgical Ltd6
2010-07-15OAIOfficial action indicatedPeregrine Surgical Ltd6
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