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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.

7 linked reportsMalfunction 7
12232025-11: 3 reports for this device2025-12: 2 reports for this device2026-01: 2 reports for this device111201
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2025-113
2025-122
2026-012
This device (reports/month)Average device in its product code (reports/device/month)
Failure-mode summaryAI-generated

7 linked report narratives available — no AI summary generated yet.

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2026-01-083005619970-2025-00076MalfunctionAvailableexact di
2026-01-083005619970-2025-00075MalfunctionAvailableexact di
2025-12-103005619970-2025-00071MalfunctionAvailableexact di
2025-12-093005619970-2025-00072MalfunctionAvailableexact di
2025-11-283005619970-2025-00067MalfunctionAvailableexact di
2025-11-283005619970-2025-00062MalfunctionAvailableexact di
2025-11-283005619970-2025-00066MalfunctionAvailableexact di
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2015-04-23NAINo action indicatedArjo (Suzhou) Co., Ltd.0
2014-03-20VAIVoluntary action indicatedARJOHUNTLEIGH POLSKA Sp. z.o.o.3
2013-02-07NAINo action indicatedARJOHUNTLEIGH AB0
2013-02-07NAINo action indicatedARJOHUNTLEIGH AB0
2012-09-06VAIVoluntary action indicatedHuntleigh Healthcare Ltd.0
2011-11-24NAINo action indicatedArjo (Suzhou) Co., Ltd.0
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