LFIT · recalls, adverse events, clearances

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.

132 linked reportsInjury 132

Monthly adverse-event reports for this device versus the product-code average.
Month	This device (reports)	Product-code average (reports per device)
2019-01	6	2.58
2019-02	3	2.2
2019-03	2	2.34
2019-04	5	2.33
2019-05	2	1.91
2019-06	3	1.65
2019-07	2	1.73
2019-08	4	1.9
2019-09	2	1.97
2019-10	4	2.11
2019-11	0	1.69
2019-12	4	1.96
2020-01	0	2.17
2020-02	3	2.16
2020-03	2	2.7
2020-04	1	1.87
2020-05	1	1.97
2020-06	2	1.7
2020-07	3	2.13
2020-08	1	1.63
2020-09	1	1.84
2020-10	1	1.97
2020-11	0	1.88
2020-12	0	1.94
2021-01	1	1.98
2021-02	2	1.7
2021-03	4	1.76
2021-04	0	1.66
2021-05	1	1.64
2021-06	2	2.05
2021-07	0	1.88
2021-08	1	1.77
2021-09	2	1.9
2021-10	3	1.8
2021-11	1	1.76
2021-12	0	1.95
2022-01	1	1.64
2022-02	2	1.94
2022-03	3	1.68
2022-04	1	1.85
2022-05	1	1.75
2022-06	2	1.8
2022-07	0	1.77
2022-08	4	1.9
2022-09	1	1.84
2022-10	1	1.78
2022-11	1	1.88
2022-12	1	1.73
2023-01	0	1.93
2023-02	2	1.75
2023-03	1	1.8
2023-04	0	1.86
2023-05	1	1.89
2023-06	0	1.94
2023-07	0	1.96
2023-08	0	1.91
2023-09	0	1.94
2023-10	2	1.48
2023-11	3	1.48
2023-12	1	1.51
2024-01	3	1.61
2024-02	1	1.74
2024-03	2	1.95
2024-04	2	1.62
2024-05	2	2.09
2024-06	2	1.85
2024-07	2	1.61
2024-08	2	1.84
2024-09	2	1.93
2024-10	1	1.6
2024-11	2	1.44
2024-12	0	1.46
2025-01	1	1.52
2025-02	1	1.38
2025-03	1	1.67
2025-04	0	1.69
2025-05	0	1.39
2025-06	1	1.63
2025-07	0	1.65
2025-08	0	1.44
2025-09	0	1.63
2025-10	0	1.64
2025-11	0	1.7
2025-12	1	1.69
2026-01	0	1.84
2026-02	1	1.46
2026-03	3	1.91
2026-04	0	1.65
2026-05	5	1.59
2026-06	0	1.56

This device (reports/month)Average device in JDI, KWY, LWJ (reports/device/month)

Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports

Date	Report #	Type	Narrative	Link basis
2026-05-28	0002249697-2026-00484	Injury	Available	exact di
2026-05-28	0002249697-2026-00480	Injury	Available	exact di
2026-05-28	0002249697-2026-00486	Injury	Available	exact di
2026-05-27	0002249697-2026-00468	Injury	Available	exact di
2026-05-27	0002249697-2026-00452	Injury	Available	exact di
2026-03-04	0002249697-2026-00171	Injury	Available	exact di
2026-03-04	0002249697-2026-00162	Injury	Available	exact di
2026-03-03	0002249697-2026-00152	Injury	Available	exact di
2026-02-25	0002249697-2026-00136	Injury	Available	exact di
2025-12-05	0002249697-2025-01416	Injury	Available	exact di
2025-06-09	0002249697-2025-00610	Injury	Available	exact di
2025-03-03	0002249697-2025-00251	Injury	Available	exact di
2025-02-06	0002249697-2025-00161	Injury	Available	exact di
2025-01-15	0002249697-2025-00086	Injury	Available	exact di
2024-11-11	0002249697-2024-01530	Injury	Available	exact di

Showing 1–15 of 132

Regulatory clearances

None linked.

Manufacturer compliance record

Date	Type	Outcome	Facility	Citations
2023-12-01	VAI	Voluntary action indicated	Howmedica Osteonics Corp.	1
2021-06-22	NAI	No action indicated	Howmedica Osteonics Corp.	0
2015-03-09	VAI	Voluntary action indicated	Howmedica Osteonics Corp.	3
2013-04-16	VAI	Voluntary action indicated	Howmedica Osteonics Corp.	3
2010-01-15	NAI	No action indicated	Howmedica Osteonics Corp.	0

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