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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.

11 linked reportsMalfunction 11
12342019-10: 0 reports for this device; peer average 2/device2021-10: 0 reports for this device; peer average 1/device2022-09: 0 reports for this device; peer average 1/device2024-05: 0 reports for this device; peer average 1/device2025-03: 0 reports for this device; peer average 2/device2025-04: 0 reports for this device; peer average 1/device2025-05: 0 reports for this device; peer average 1.5/device2025-06: 0 reports for this device; peer average 2/device2025-07: 0 reports for this device; peer average 2.5/device2025-08: 0 reports for this device; peer average 4/device2025-09: 0 reports for this device; peer average 1/device2025-11: 2 reports for this device; peer average 2/device2025-12: 3 reports for this device; peer average 2.67/device2026-01: 4 reports for this device; peer average 3/device2026-02: 2 reports for this device; peer average 2/device101009050304050607080911120102
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-1002
2021-1001
2022-0901
2024-0501
2025-0302
2025-0401
2025-0501.5
2025-0602
2025-0702.5
2025-0804
2025-0901
2025-1122
2025-1232.67
2026-0143
2026-0222
This device (reports/month)Average device in LWG (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2026-02-051043572-2026-00016MalfunctionAvailablecatalog number
2026-01-151043572-2026-00007MalfunctionAvailablecatalog number
2026-01-0623973556MalfunctionAvailablecatalog number
2025-12-181043572-2025-00117MalfunctionAvailablecatalog number
2025-12-181043572-2025-00119MalfunctionAvailableexact di
2025-11-1823582428MalfunctionAvailablecatalog number

Showing the most recent 6 of 11 linked reports.

Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2026-04-16NAINo action indicatedSteris Corporation0
2026-04-16NAINo action indicatedSteris Corporation0
2026-04-03NAINo action indicatedIsomedix Operations Inc.0
2026-03-12NAINo action indicatedIsomedix Operations Inc0
2026-02-26VAIVoluntary action indicatedSteris S.p.A.1
2026-02-12VAIVoluntary action indicatedSynergy Health Ede BV2
2026-02-12NAINo action indicatedSynergy Health Marseille0
2025-12-12OAIOfficial action indicatedBlack Diamond Video Inc.3
2025-08-01VAIVoluntary action indicatedSTERIS Laboratories, Inc.2
2025-06-18NAINo action indicatedIsomedix Operations Inc.0
2025-06-17NAINo action indicatedIsomedix Operations Inc0
2025-06-05NAINo action indicatedIsomedix Operations, Inc.0
2025-04-01NAINo action indicatedSteris Corporation0
2025-02-21NAINo action indicatedIsomedix Operations Inc.0
2025-01-23NAINo action indicatedSynergy Health Allershausen GmbH0
2024-12-12VAIVoluntary action indicatedIsomedix Operations, Inc0
2024-12-05NAINo action indicatedSteris (Synergy Health Ede BV)0
2024-11-21VAIVoluntary action indicatedSteris Applied Sterilization Technologies ULC2
2024-09-23NAINo action indicatedIsomedix Operations, Inc.0
2024-09-19NAINo action indicatedIsomedix Operations, Inc.0
2015-02-20WLWarning LetterKey Surgical LLC
2014-05-22WLWarning LetterIsomedix Operations, Inc.
2012-05-29WLWarning LetterAlbert Browne Ltd.
2011-02-09WLWarning LetterSteris Corporation
2011-02-09WLWarning LetterSteris Corporation
2010-09-27WLWarning LetterIsomedix Operations, Inc.
2010-04-20INJInjunctionSteris Corporation
2010-04-20INJInjunctionSteris Corporation
2009-07-31WLWarning LetterMedivators Inc