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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.

2 linked reportsMalfunction 2
4711142019-02: 2 reports for this device; peer average 2/device2019-04: 0 reports for this device; peer average 2/device2019-08: 0 reports for this device; peer average 2/device2020-05: 0 reports for this device; peer average 2/device2020-07: 0 reports for this device; peer average 4/device2020-12: 0 reports for this device; peer average 3/device2021-01: 0 reports for this device; peer average 1.5/device2021-02: 0 reports for this device; peer average 2/device2021-03: 0 reports for this device; peer average 14/device2021-04: 0 reports for this device; peer average 3/device2021-09: 0 reports for this device; peer average 1.67/device2021-11: 0 reports for this device; peer average 3/device2022-04: 0 reports for this device; peer average 3/device2022-09: 0 reports for this device; peer average 3/device2022-10: 0 reports for this device; peer average 3/device2023-02: 0 reports for this device; peer average 1/device2023-06: 0 reports for this device; peer average 1/device2023-11: 0 reports for this device; peer average 2/device2024-01: 0 reports for this device; peer average 1/device2024-04: 0 reports for this device; peer average 1/device2024-08: 0 reports for this device; peer average 1/device2025-01: 0 reports for this device; peer average 1/device2025-03: 0 reports for this device; peer average 1/device2025-12: 0 reports for this device; peer average 1/device2026-05: 0 reports for this device; peer average 1/device02040805071201020304091104091002061101040801031205
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0222
2019-0402
2019-0802
2020-0502
2020-0704
2020-1203
2021-0101.5
2021-0202
2021-03014
2021-0403
2021-0901.67
2021-1103
2022-0403
2022-0903
2022-1003
2023-0201
2023-0601
2023-1102
2024-0101
2024-0401
2024-0801
2025-0101
2025-0301
2025-1201
2026-0501
This device (reports/month)Average device in GDX (reports/device/month)
Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2019-02-209610612-2019-00098MalfunctionAvailablecatalog number

Showing the most recent 1 of 2 linked reports.

Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2025-07-11NAINo action indicatedAesculap Inc0
2025-07-11NAINo action indicatedAesculap Inc0
2022-07-21NAINo action indicatedAesculap AG0
2022-07-21NAINo action indicatedAesculap AG0
2021-08-11VAIVoluntary action indicatedAesculap Inc3
2021-08-11VAIVoluntary action indicatedAesculap Inc3
2018-06-13VAIVoluntary action indicatedAesculap Inc0
2018-06-13VAIVoluntary action indicatedAesculap Inc0
2016-09-22NAINo action indicatedAesculap AG0
2016-09-22NAINo action indicatedAesculap AG0
2016-09-14VAIVoluntary action indicatedAesculap Inc0
2016-09-14VAIVoluntary action indicatedAesculap Inc0
2016-07-13NAINo action indicatedAesculap Inc0
2016-07-13NAINo action indicatedAesculap Inc0
2015-07-16NAINo action indicatedAesculap AG1
2015-07-16NAINo action indicatedAesculap AG1
2015-05-05NAINo action indicatedAesculap Inc0
2015-05-05NAINo action indicatedAesculap Inc0
2014-10-23NAINo action indicatedAesculap Inc0
2014-10-23NAINo action indicatedAesculap Inc0
2011-09-26WLWarning LetterAesculap AG
2011-09-26WLWarning LetterAesculap AG
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