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.
7 linked reportsMalfunction 6Injury 1
Monthly adverse-event reports for this device versus the product-code average.
Month
This device (reports)
Product-code average (reports per device)
2019-01
0
1.5
2019-03
0
2.71
2019-04
0
1.67
2019-05
4
3
2019-06
3
1.8
2019-07
0
1.6
2019-08
0
2
2019-09
0
1.5
2019-12
0
12
2020-01
0
3
2020-02
0
1.67
2020-03
0
4
2020-04
0
1.75
2020-05
0
2.57
2020-06
0
2.88
2020-07
0
3
2020-08
0
2
2020-09
0
2
2020-10
0
2.29
2020-11
0
2.25
2020-12
0
3
2021-02
0
1
2021-03
0
2.5
2021-04
0
7
2021-05
0
1.33
2021-06
0
2
2021-07
0
1.2
2021-08
0
2.6
2021-09
0
2
2021-10
0
1
2021-11
0
1
2021-12
0
1.2
2022-01
0
2.67
2022-02
0
6
2022-03
0
6
2022-04
0
1
2022-05
0
1.5
2022-06
0
1
2022-07
0
1.5
2022-08
0
2
2022-09
0
2
2022-12
0
3.75
2023-01
0
2
2023-02
0
2
2023-03
0
4.5
2023-05
0
1
2023-06
0
9.4
2023-07
0
1.25
2023-08
0
1
2023-09
0
2
2023-10
0
1
2023-11
0
1
2023-12
0
1.33
2024-01
0
2
2024-02
0
2
2024-04
0
3.33
2024-06
0
1.33
2024-07
0
1
2024-08
0
1.25
2024-10
0
6
2024-12
0
1
2025-01
0
1
2025-03
0
2
2025-04
0
1
2025-05
0
4
2025-07
0
4.5
2025-10
0
2
2026-01
0
2
2026-05
0
2.67
This device (reports/month)Average device in HBW (reports/device/month)
Failure-mode summaryAI-generated
7 linked report narratives available — no AI summary generated yet.
Lineage each submission cites, walked transitively (indented = the cited device's own predicates). Extracted from public 510(k) summary text — heuristic, and includes reference devices mentioned alongside true predicates.