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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.

14 linked reportsMalfunction 14
61218242019-08: 0 reports for this device; peer average 2/device2020-04: 0 reports for this device; peer average 2/device2020-09: 0 reports for this device; peer average 1/device2020-12: 0 reports for this device; peer average 2/device2021-05: 0 reports for this device; peer average 2/device2021-07: 0 reports for this device; peer average 3/device2021-09: 0 reports for this device; peer average 1/device2021-11: 0 reports for this device; peer average 3/device2021-12: 0 reports for this device; peer average 1/device2022-02: 0 reports for this device; peer average 1/device2022-07: 0 reports for this device; peer average 1/device2023-01: 0 reports for this device; peer average 2/device2023-02: 1 reports for this device; peer average 23.5/device2023-03: 0 reports for this device; peer average 15/device2023-04: 0 reports for this device; peer average 6/device2023-05: 0 reports for this device; peer average 2/device2023-06: 0 reports for this device; peer average 1/device2023-07: 0 reports for this device; peer average 1/device2023-08: 0 reports for this device; peer average 1/device2023-10: 0 reports for this device; peer average 9/device2024-01: 1 reports for this device; peer average 8.67/device2024-02: 0 reports for this device; peer average 1/device2024-03: 0 reports for this device; peer average 9/device2024-04: 0 reports for this device; peer average 3.5/device2024-05: 0 reports for this device; peer average 1/device2024-06: 0 reports for this device; peer average 2/device2024-09: 0 reports for this device; peer average 1/device2024-10: 0 reports for this device; peer average 1/device2025-01: 0 reports for this device; peer average 3/device2025-02: 0 reports for this device; peer average 2.67/device2025-03: 0 reports for this device; peer average 1/device2025-04: 3 reports for this device; peer average 1.5/device2025-05: 0 reports for this device; peer average 1.5/device2025-08: 0 reports for this device; peer average 1.33/device2025-10: 2 reports for this device; peer average 1.5/device2025-11: 1 reports for this device; peer average 1/device2025-12: 6 reports for this device; peer average 6/device2026-01: 0 reports for this device; peer average 6/device2026-02: 0 reports for this device; peer average 1.5/device2026-03: 0 reports for this device; peer average 4.4/device2026-04: 0 reports for this device; peer average 5.33/device2026-05: 0 reports for this device; peer average 2.2/device2026-06: 0 reports for this device; peer average 4/device08040912050709111202070102030405060708100102030405060910010203040508101112010203040506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0802
2020-0402
2020-0901
2020-1202
2021-0502
2021-0703
2021-0901
2021-1103
2021-1201
2022-0201
2022-0701
2023-0102
2023-02123.5
2023-03015
2023-0406
2023-0502
2023-0601
2023-0701
2023-0801
2023-1009
2024-0118.67
2024-0201
2024-0309
2024-0403.5
2024-0501
2024-0602
2024-0901
2024-1001
2025-0103
2025-0202.67
2025-0301
2025-0431.5
2025-0501.5
2025-0801.33
2025-1021.5
2025-1111
2025-1266
2026-0106
2026-0201.5
2026-0304.4
2026-0405.33
2026-0502.2
2026-0604
This device (reports/month)Average device in FTA (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2025-12-231043572-2025-00123MalfunctionAvailablecatalog number
2025-12-111043572-2025-00110MalfunctionAvailablecatalog number
2025-11-07MW5178603MalfunctionAvailablecatalog number
2025-10-311043572-2025-00096MalfunctionAvailablecatalog number
2025-04-181043572-2025-00043MalfunctionAvailablecatalog number
2024-01-181043572-2024-00006MalfunctionAvailableexact di
2023-02-081043572-2023-00011MalfunctionAvailableexact di

Showing the most recent 7 of 14 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
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