DJO SURGICAL · 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.

31 linked reportsInjury 31

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	1.68
2019-02	0	1.59
2019-03	0	1.68
2019-04	0	1.52
2019-05	0	1.76
2019-06	0	1.87
2019-07	2	1.41
2019-08	2	1.97
2019-09	0	1.48
2019-10	0	1.8
2019-11	0	1.62
2019-12	2	1.74
2020-01	0	1.89
2020-02	0	2.15
2020-03	0	1.76
2020-04	0	1.72
2020-05	0	1.43
2020-06	0	1.8
2020-07	0	1.91
2020-08	0	1.63
2020-09	0	1.92
2020-10	0	2.1
2020-11	0	1.85
2020-12	0	1.82
2021-01	0	1.95
2021-02	0	1.82
2021-03	0	1.98
2021-04	0	1.76
2021-05	0	1.76
2021-06	6	1.63
2021-07	0	1.87
2021-08	2	2.03
2021-09	0	1.66
2021-10	0	1.71
2021-11	0	1.97
2021-12	0	1.93
2022-01	0	2.04
2022-02	0	2.04
2022-03	0	1.73
2022-04	0	2.04
2022-05	2	1.88
2022-06	0	2.01
2022-07	0	2.05
2022-08	0	2
2022-09	2	1.84
2022-10	0	1.87
2022-11	0	2.02
2022-12	0	1.82
2023-01	2	1.72
2023-02	0	1.94
2023-03	0	1.93
2023-04	0	1.92
2023-05	2	2
2023-06	0	2.26
2023-07	0	2.07
2023-08	0	1.67
2023-09	0	1.51
2023-10	0	1.56
2023-11	0	1.61
2023-12	0	1.41
2024-01	0	1.99
2024-02	0	1.76
2024-03	0	1.68
2024-04	0	1.77
2024-05	0	1.72
2024-06	0	1.9
2024-07	0	1.6
2024-08	0	1.7
2024-09	1	1.71
2024-10	2	1.61
2024-11	0	1.58
2024-12	0	1.63
2025-01	1	1.72
2025-02	1	1.56
2025-03	0	1.84
2025-04	0	1.63
2025-05	1	1.75
2025-06	0	1.83
2025-07	0	1.71
2025-08	0	1.53
2025-09	0	1.51
2025-10	1	1.62
2025-11	1	1.71
2025-12	0	2.11
2026-01	1	1.87
2026-02	0	1.8
2026-03	0	1.75
2026-04	0	1.7
2026-05	0	1.75
2026-06	0	1.68

This device (reports/month)Average device in KWS (reports/device/month)

Failure-mode summaryAI-generated

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

Recall history

No recalls linked.

Individual MAUDE reports

Date	Report #	Type	Narrative	Link basis
2026-01-20	1644408-2026-00100	Injury	Available	exact di
2025-11-26	1644408-2025-01812	Injury	Available	exact di
2025-10-17	1644408-2025-01511	Injury	Available	exact di
2025-05-24	1644408-2025-00671	Injury	Available	exact di
2025-02-25	1644408-2025-00227	Injury	Available	exact di
2025-01-16	1644408-2024-02137	Injury	Available	exact di
2024-10-24	1644408-2024-01649	Injury	Available	exact di
2024-10-22	1644408-2024-01631	Injury	Available	exact di
2024-09-06	1644408-2024-01370	Injury	Available	exact di
2023-05-19	1644408-2023-00721	Injury	Available	exact di
2023-01-26	1644408-2023-00109	Injury	Available	exact di
2022-09-08	1644408-2022-01189	Injury	Available	exact di
2022-05-04	1644408-2022-00555	Injury	Available	exact di
2021-08-18	1644408-2021-00847	Injury	Available	exact di
2021-06-30	1644408-2021-00652	Injury	Available	exact di

Showing the most recent 20 of 31 linked reports.

Showing 1–15 of 20

Regulatory clearances

Predicate lineage

K123982
- K080402

Cited as predicate by: K162024, K172054, K243955, K251558, K260802

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.

Manufacturer compliance record

Date	Type	Outcome	Facility	Citations
2021-10-28	VAI	Voluntary action indicated	Encore Medical, LP	2
2020-03-11	NAI	No action indicated	Encore Medical, LP	0
2015-07-24	NAI	No action indicated	Encore Medical, LP	0
2013-06-28	VAI	Voluntary action indicated	Encore Medical, LP	2

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