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.
48 linked reportsInjury 32Malfunction 16
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2019-02 | 0 | 1 |
| 2019-04 | 0 | 1 |
| 2019-05 | 0 | 1 |
| 2019-06 | 0 | 1.33 |
| 2019-07 | 0 | 1 |
| 2019-08 | 0 | 1 |
| 2019-09 | 0 | 1.5 |
| 2019-10 | 0 | 1 |
| 2019-12 | 1 | 1.5 |
| 2020-01 | 0 | 1 |
| 2020-02 | 1 | 1 |
| 2020-03 | 0 | 1.4 |
| 2020-04 | 0 | 1.4 |
| 2020-05 | 0 | 1 |
| 2020-06 | 0 | 1 |
| 2020-07 | 3 | 4.5 |
| 2020-08 | 0 | 2 |
| 2020-09 | 3 | 3 |
| 2020-10 | 0 | 4.5 |
| 2020-11 | 0 | 1 |
| 2020-12 | 0 | 2 |
| 2021-01 | 0 | 3.14 |
| 2021-03 | 3 | 2.75 |
| 2021-04 | 0 | 1.33 |
| 2021-05 | 5 | 3.14 |
| 2021-06 | 6 | 3.67 |
| 2021-07 | 0 | 2 |
| 2021-08 | 6 | 3.25 |
| 2021-09 | 0 | 1.8 |
| 2021-10 | 0 | 4 |
| 2021-11 | 3 | 4.5 |
| 2021-12 | 0 | 3 |
| 2022-01 | 0 | 1 |
| 2022-02 | 0 | 2.5 |
| 2022-03 | 0 | 2.75 |
| 2022-04 | 0 | 1 |
| 2022-05 | 0 | 2.33 |
| 2022-06 | 0 | 2.5 |
| 2022-07 | 3 | 2.17 |
| 2022-08 | 0 | 2.29 |
| 2022-09 | 0 | 2.86 |
| 2022-10 | 0 | 3.25 |
| 2022-11 | 0 | 2.5 |
| 2022-12 | 6 | 3.4 |
| 2023-01 | 0 | 2 |
| 2023-02 | 0 | 2 |
| 2023-03 | 0 | 1.5 |
| 2023-05 | 0 | 2.5 |
| 2023-06 | 0 | 1 |
| 2023-07 | 0 | 1.5 |
| 2023-08 | 0 | 2.2 |
| 2023-09 | 0 | 2 |
| 2023-10 | 0 | 1.67 |
| 2023-11 | 0 | 1.67 |
| 2023-12 | 0 | 2.33 |
| 2024-01 | 0 | 1.33 |
| 2024-02 | 0 | 1.67 |
| 2024-03 | 4 | 3.25 |
| 2024-04 | 0 | 3 |
| 2024-05 | 0 | 2 |
| 2024-06 | 0 | 2.25 |
| 2024-08 | 0 | 1.6 |
| 2024-09 | 2 | 1.75 |
| 2024-10 | 0 | 2.33 |
| 2024-11 | 0 | 5.67 |
| 2024-12 | 0 | 8.67 |
| 2025-01 | 0 | 2.6 |
| 2025-02 | 0 | 7 |
| 2025-03 | 0 | 5.33 |
| 2025-04 | 0 | 4.25 |
| 2025-05 | 0 | 3.33 |
| 2025-06 | 0 | 5 |
| 2025-07 | 0 | 2 |
| 2025-08 | 0 | 1.83 |
| 2025-09 | 0 | 3.17 |
| 2025-10 | 0 | 2.44 |
| 2025-11 | 0 | 3.8 |
| 2025-12 | 0 | 4.33 |
| 2026-01 | 2 | 1.5 |
| 2026-02 | 0 | 3.8 |
| 2026-03 | 0 | 2.8 |
| 2026-04 | 0 | 4 |
| 2026-05 | 0 | 17 |
| 2026-06 | 0 | 2 |
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 |
|---|---|---|---|---|
| 2026-01-30 | 1219602-2026-00271 | Malfunction | Available | catalog number |
| 2024-09-24 | 1219602-2024-02087 | Malfunction | Available | catalog number |
| 2024-03-20 | 1219602-2024-00558 | Malfunction | Available | catalog number |
| 2024-03-07 | 1219602-2024-00415 | Malfunction | Available | catalog number |
| 2022-12-16 | 1219602-2022-01986 | Injury | Available | catalog number |
| 2022-12-13 | 1219602-2022-01965 | Injury | Available | catalog number |
| 2022-07-20 | 1219602-2022-01038 | Injury | Available | catalog number |
| 2021-11-25 | 1219602-2021-02577 | Injury | Available | catalog number |
| 2021-08-17 | 1219602-2021-01731 | Injury | Available | catalog number |
| 2021-08-10 | 1219602-2021-01693 | Injury | Available | catalog number |
| 2021-06-10 | 1219602-2021-01331 | Malfunction | Available | catalog number |
| 2021-06-09 | 1219602-2021-01327 | Malfunction | Available | catalog number |
| 2021-05-06 | 1219602-2021-01045 | Injury | Available | catalog number |
| 2021-05-06 | 1219602-2021-01052 | Injury | Available | catalog number |
| 2021-05-06 | 1219602-2021-01054 | Injury | Available | catalog number |
Showing the most recent 20 of 48 linked reports.
Showing 1–15 of 20
Regulatory clearances
None linked.
Manufacturer compliance record
| Date | Type | Outcome | Facility | Citations |
|---|---|---|---|---|
| 2025-01-27 | NAI | No action indicated | Integrity Orthopaedics Inc | 0 |
| 2023-05-03 | NAI | No action indicated | CARTIHEAL, LTD | 0 |
| 2021-12-09 | VAI | Voluntary action indicated | Smith & Nephew, Inc. | 1 |
| 2021-12-09 | VAI | Voluntary action indicated | Smith & Nephew, Inc. | 1 |
| 2021-10-26 | NAI | No action indicated | Smith & Nephew Inc. | 0 |
| 2021-10-26 | NAI | No action indicated | Smith & Nephew Inc. | 0 |
| 2020-02-06 | VAI | Voluntary action indicated | Blue Belt Technologies, Inc | 6 |
| 2019-10-25 | NAI | No action indicated | Tusker Medical, Inc. | 0 |
| 2019-10-08 | VAI | Voluntary action indicated | Tusker Medical, Inc. | 3 |
| 2018-03-30 | NAI | No action indicated | Ascension Orthopedics, Inc | 0 |
| 2018-02-02 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2018-02-02 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2018-01-30 | NAI | No action indicated | Smith & Nephew | 0 |
| 2017-08-21 | NAI | No action indicated | Smith & Nephew, Inc. Advanced Surgical Devices Division | 0 |
| 2017-08-02 | VAI | Voluntary action indicated | Smith & Nephew, Inc. | 3 |
| 2017-08-02 | VAI | Voluntary action indicated | Smith & Nephew, Inc. | 3 |
| 2017-07-24 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2017-07-24 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2017-05-25 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2017-05-25 | NAI | No action indicated | Smith & Nephew, Inc. | 0 |
| 2015-04-30 | WL | Warning Letter | Smith & Nephew Inc. | — |
| 2015-04-30 | WL | Warning Letter | Smith & Nephew Inc. | — |
| 2014-06-11 | WL | Warning Letter | Smith & Nephew, Inc. | — |
| 2010-09-16 | WL | Warning Letter | Ascension Orthopedics, Inc | — |
Similar devices
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
- 3P Hip System ORTHOPEDIATRICS CORP.
Select up to two to place side-by-side with this device.