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 reportsInjury 2
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-02
0
1
2019-04
0
1.5
2019-05
0
1.5
2019-06
0
2
2019-07
0
4
2019-08
0
2
2019-09
0
2
2019-10
0
1.5
2019-12
0
1
2020-01
0
1
2020-06
0
1
2020-08
0
1
2020-12
0
1
2021-01
0
1
2021-02
0
1
2021-03
0
1
2021-04
0
1
2021-06
0
1
2021-09
0
1
2021-11
0
1
2021-12
0
1.5
2022-01
0
2
2022-02
0
1
2022-03
0
2
2022-04
0
1
2022-05
0
1
2022-06
0
1
2022-07
0
1
2022-09
1
1
2022-10
0
1
2022-12
1
1.25
2023-01
0
1
2023-02
0
1
2023-03
0
1.5
2023-04
0
1
2023-05
0
1
2023-11
0
1
2024-01
0
1
2024-02
0
2
2024-03
0
1
2024-04
0
1
2024-05
0
1.67
2024-06
0
1
2024-09
0
1
2024-10
0
1
2024-11
0
1
2025-01
0
1
2025-02
0
1
2025-05
0
1
2025-06
0
1
2025-07
0
1
2025-09
0
1
2025-10
0
1
2025-11
0
1
2026-01
0
1
2026-02
0
3
2026-03
0
3.67
2026-04
0
3.33
2026-05
0
2.67
2026-06
0
1.5
This device (reports/month)Average device in IRT (reports/device/month)
Failure-mode summaryAI-generated
2 linked report narratives available — no AI summary generated yet.