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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.

1 linked reportMalfunction 1
24572019-01: 0 reports for this device; peer average 2/device2019-03: 0 reports for this device; peer average 1/device2019-06: 0 reports for this device; peer average 1/device2019-10: 0 reports for this device; peer average 1/device2019-12: 0 reports for this device; peer average 1/device2020-02: 0 reports for this device; peer average 2/device2020-03: 0 reports for this device; peer average 2/device2020-07: 0 reports for this device; peer average 3/device2020-09: 0 reports for this device; peer average 2.5/device2021-02: 0 reports for this device; peer average 3/device2021-04: 0 reports for this device; peer average 2/device2021-05: 0 reports for this device; peer average 1.33/device2021-06: 0 reports for this device; peer average 1/device2021-08: 0 reports for this device; peer average 1/device2021-10: 0 reports for this device; peer average 3/device2021-11: 1 reports for this device; peer average 1/device2021-12: 0 reports for this device; peer average 2/device2022-02: 0 reports for this device; peer average 1/device2022-06: 0 reports for this device; peer average 7/device2022-09: 0 reports for this device; peer average 1/device2023-03: 0 reports for this device; peer average 3/device2023-05: 0 reports for this device; peer average 3/device2023-08: 0 reports for this device; peer average 2/device2024-01: 0 reports for this device; peer average 1/device2024-06: 0 reports for this device; peer average 3/device2024-07: 0 reports for this device; peer average 2/device2024-08: 0 reports for this device; peer average 1/device2024-10: 0 reports for this device; peer average 1/device2025-05: 0 reports for this device; peer average 2/device2025-07: 0 reports for this device; peer average 2/device2025-08: 0 reports for this device; peer average 2/device2026-02: 0 reports for this device; peer average 2/device2026-03: 0 reports for this device; peer average 3/device2026-05: 0 reports for this device; peer average 1.71/device2026-06: 0 reports for this device; peer average 3.25/device0103061012020307090204050608101112020609030508010607081005070802030506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0102
2019-0301
2019-0601
2019-1001
2019-1201
2020-0202
2020-0302
2020-0703
2020-0902.5
2021-0203
2021-0402
2021-0501.33
2021-0601
2021-0801
2021-1003
2021-1111
2021-1202
2022-0201
2022-0607
2022-0901
2023-0303
2023-0503
2023-0802
2024-0101
2024-0603
2024-0702
2024-0801
2024-1001
2025-0502
2025-0702
2025-0802
2026-0202
2026-0303
2026-0501.71
2026-0603.25
This device (reports/month)Average device in FRL (reports/device/month)
Failure-mode summaryAI-generated

1 linked report narrative available — no AI summary generated yet.

Recall history

No recalls linked.

Individual MAUDE reports
DateReport #TypeNarrativeLink basis
2021-11-303014527682-2021-00021MalfunctionAvailablecatalog number
Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2025-09-05VAIVoluntary action indicatedA Plus International, Inc1
2025-09-05VAIVoluntary action indicatedA Plus International, Inc1
2017-03-08NAINo action indicatedA Plus International, Inc0
2017-03-08NAINo action indicatedA Plus International, Inc0
2013-11-06NAINo action indicatedA Plus International, Inc0
2013-11-06NAINo action indicatedA Plus International, Inc0
2013-04-04VAIVoluntary action indicatedA Plus International, Inc6
2013-04-04VAIVoluntary action indicatedA Plus International, Inc6