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.
2 linked reportsInjury 2
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2019-01 | 0 | 3.11 |
| 2019-02 | 0 | 2.65 |
| 2019-03 | 0 | 2.75 |
| 2019-04 | 0 | 2.72 |
| 2019-05 | 0 | 2.21 |
| 2019-06 | 0 | 2.12 |
| 2019-07 | 0 | 2.1 |
| 2019-08 | 0 | 2.3 |
| 2019-09 | 0 | 2.46 |
| 2019-10 | 0 | 2.79 |
| 2019-11 | 0 | 2.66 |
| 2019-12 | 0 | 2.62 |
| 2020-01 | 0 | 2.83 |
| 2020-02 | 0 | 2.85 |
| 2020-03 | 0 | 3.06 |
| 2020-04 | 0 | 2.39 |
| 2020-05 | 0 | 2.22 |
| 2020-06 | 0 | 2.19 |
| 2020-07 | 0 | 2.73 |
| 2020-08 | 0 | 2.44 |
| 2020-09 | 0 | 2.52 |
| 2020-10 | 0 | 2.86 |
| 2020-11 | 0 | 2.72 |
| 2020-12 | 0 | 2.76 |
| 2021-01 | 0 | 2.58 |
| 2021-02 | 0 | 2.33 |
| 2021-03 | 0 | 2.4 |
| 2021-04 | 0 | 2.34 |
| 2021-05 | 0 | 2.24 |
| 2021-06 | 0 | 2.48 |
| 2021-07 | 0 | 2.38 |
| 2021-08 | 0 | 2.19 |
| 2021-09 | 0 | 2.42 |
| 2021-10 | 0 | 2.14 |
| 2021-11 | 0 | 2.3 |
| 2021-12 | 0 | 2.49 |
| 2022-01 | 0 | 2.15 |
| 2022-02 | 0 | 2.31 |
| 2022-03 | 0 | 2.23 |
| 2022-04 | 0 | 2.23 |
| 2022-05 | 0 | 2.25 |
| 2022-06 | 0 | 2.28 |
| 2022-07 | 0 | 2.15 |
| 2022-08 | 0 | 2.22 |
| 2022-09 | 0 | 2.28 |
| 2022-10 | 0 | 2.23 |
| 2022-11 | 0 | 2.31 |
| 2022-12 | 0 | 2.14 |
| 2023-01 | 0 | 2.2 |
| 2023-02 | 0 | 2.26 |
| 2023-03 | 0 | 2.4 |
| 2023-04 | 0 | 2.34 |
| 2023-05 | 0 | 2.39 |
| 2023-06 | 0 | 2.35 |
| 2023-07 | 0 | 2.11 |
| 2023-08 | 0 | 1.94 |
| 2023-09 | 0 | 1.96 |
| 2023-10 | 0 | 1.7 |
| 2023-11 | 0 | 1.7 |
| 2023-12 | 0 | 1.76 |
| 2024-01 | 0 | 1.71 |
| 2024-02 | 0 | 1.98 |
| 2024-03 | 0 | 1.92 |
| 2024-04 | 0 | 1.73 |
| 2024-05 | 0 | 2.02 |
| 2024-06 | 0 | 1.99 |
| 2024-07 | 0 | 1.84 |
| 2024-08 | 0 | 2.1 |
| 2024-09 | 0 | 2.07 |
| 2024-10 | 0 | 1.93 |
| 2024-11 | 0 | 1.9 |
| 2024-12 | 0 | 1.84 |
| 2025-01 | 0 | 2.16 |
| 2025-02 | 0 | 1.69 |
| 2025-03 | 0 | 1.83 |
| 2025-04 | 0 | 1.78 |
| 2025-05 | 0 | 1.73 |
| 2025-06 | 0 | 1.85 |
| 2025-07 | 0 | 1.76 |
| 2025-08 | 0 | 1.68 |
| 2025-09 | 0 | 1.77 |
| 2025-10 | 0 | 1.62 |
| 2025-11 | 0 | 1.8 |
| 2025-12 | 0 | 1.83 |
| 2026-01 | 2 | 1.87 |
| 2026-02 | 0 | 1.61 |
| 2026-03 | 0 | 2.04 |
| 2026-04 | 0 | 1.83 |
| 2026-05 | 0 | 1.74 |
| 2026-06 | 0 | 1.76 |
Failure-mode summaryAI-generated
2 linked report narratives available — no AI summary generated yet.
Recall history
| Initiated | Recall # | Class | Status | Reason | Quantity | Link basis |
|---|---|---|---|---|---|---|
| 2020-11-25 | Z-0627-2021 | Class II | Terminated | Specific lots of multiple sterile medical devices may have a breach in the sterile seal. A breach in the packaging seal could lead to loss of sterility of the device.Distribution: Worldwide distribution. US nationwide, ARGENTINA, AUSTRALIA, Brazil, CANADA, CHILE, CHINA, COSTA RICA, EMEA, HONG KONG, INDIA, JAPAN, KOREA, MALAYSIA, NEW ZEALAND, SINGAPORE, and TAIWAN | 7428 | clearance family |
Individual MAUDE reports
| Date | Report # | Type | Narrative | Link basis |
|---|---|---|---|---|
| 2026-01-09 | 0001825034-2026-00085 | Injury | Available | exact di |
| 2026-01-09 | 0001825034-2026-00084 | Injury | Available | exact di |
Regulatory clearances
Predicate lineage
K082446
Cited as predicate by: K113271
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
None in the loaded window.
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