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.
18 linked reportsInjury 14Malfunction 4
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2019-01 | 0 | 3.05 |
| 2019-02 | 0 | 2.66 |
| 2019-03 | 0 | 3.06 |
| 2019-04 | 0 | 2.86 |
| 2019-05 | 0 | 2.21 |
| 2019-06 | 0 | 1.9 |
| 2019-07 | 0 | 1.87 |
| 2019-08 | 0 | 2.21 |
| 2019-09 | 0 | 2.46 |
| 2019-10 | 0 | 2.72 |
| 2019-11 | 0 | 2.27 |
| 2019-12 | 0 | 2.6 |
| 2020-01 | 0 | 3.01 |
| 2020-02 | 0 | 2.58 |
| 2020-03 | 0 | 3.26 |
| 2020-04 | 0 | 2.33 |
| 2020-05 | 0 | 2.25 |
| 2020-06 | 0 | 2.15 |
| 2020-07 | 0 | 2.55 |
| 2020-08 | 1 | 2.1 |
| 2020-09 | 0 | 2.7 |
| 2020-10 | 0 | 2.61 |
| 2020-11 | 0 | 2.42 |
| 2020-12 | 0 | 2.43 |
| 2021-01 | 0 | 2.59 |
| 2021-02 | 0 | 2.13 |
| 2021-03 | 0 | 2.12 |
| 2021-04 | 0 | 2.15 |
| 2021-05 | 0 | 2.05 |
| 2021-06 | 0 | 2.56 |
| 2021-07 | 0 | 2.42 |
| 2021-08 | 1 | 2.45 |
| 2021-09 | 0 | 2.52 |
| 2021-10 | 0 | 2.28 |
| 2021-11 | 0 | 2.14 |
| 2021-12 | 0 | 2.39 |
| 2022-01 | 0 | 2.18 |
| 2022-02 | 1 | 2.04 |
| 2022-03 | 0 | 2.29 |
| 2022-04 | 0 | 2.2 |
| 2022-05 | 0 | 2.22 |
| 2022-06 | 3 | 2.34 |
| 2022-07 | 0 | 2.16 |
| 2022-08 | 0 | 2.22 |
| 2022-09 | 0 | 2.27 |
| 2022-10 | 1 | 2.21 |
| 2022-11 | 0 | 2.27 |
| 2022-12 | 0 | 2.3 |
| 2023-01 | 1 | 2.46 |
| 2023-02 | 1 | 2.22 |
| 2023-03 | 0 | 2.47 |
| 2023-04 | 0 | 2.35 |
| 2023-05 | 1 | 2.23 |
| 2023-06 | 0 | 2.28 |
| 2023-07 | 0 | 2.11 |
| 2023-08 | 0 | 1.94 |
| 2023-09 | 0 | 1.93 |
| 2023-10 | 0 | 1.71 |
| 2023-11 | 0 | 1.65 |
| 2023-12 | 0 | 1.77 |
| 2024-01 | 0 | 1.79 |
| 2024-02 | 0 | 2.09 |
| 2024-03 | 0 | 1.93 |
| 2024-04 | 0 | 1.78 |
| 2024-05 | 0 | 2 |
| 2024-06 | 0 | 1.88 |
| 2024-07 | 0 | 1.73 |
| 2024-08 | 0 | 1.86 |
| 2024-09 | 0 | 2 |
| 2024-10 | 1 | 1.81 |
| 2024-11 | 0 | 1.84 |
| 2024-12 | 1 | 1.59 |
| 2025-01 | 0 | 2.01 |
| 2025-02 | 0 | 1.56 |
| 2025-03 | 0 | 1.83 |
| 2025-04 | 0 | 1.84 |
| 2025-05 | 0 | 1.78 |
| 2025-06 | 0 | 1.87 |
| 2025-07 | 0 | 1.86 |
| 2025-08 | 1 | 1.76 |
| 2025-09 | 0 | 1.73 |
| 2025-10 | 0 | 1.75 |
| 2025-11 | 3 | 1.8 |
| 2025-12 | 1 | 1.92 |
| 2026-01 | 1 | 1.96 |
| 2026-02 | 0 | 1.66 |
| 2026-03 | 0 | 1.9 |
| 2026-04 | 0 | 1.94 |
| 2026-05 | 0 | 1.68 |
| 2026-06 | 0 | 1.73 |
Failure-mode summaryAI-generated
18 linked report narratives available — no AI summary generated yet.
Recall history
| Initiated | Recall # | Class | Status | Reason | Quantity | Link basis |
|---|---|---|---|---|---|---|
| 2025-09-26 | Z-0419-2026 | Class II | Open, Classified | Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E Bearing due to a commingle. The outer package is labeled as a Size F 44 mm, however, the implant inside the package is a Size G 46 mm, and vice versa.Distribution: US: OH, GA, WI, NE, IA, IL, CA, NY, MD, NC, PA, AL, TN, MI, WA, FL, TX, KS, NM, AZ, and CANADA, AUSTRALIA, NETHERLANDS | 63 units | code info di |
Individual MAUDE reports
| Date | Report # | Type | Narrative | Link basis |
|---|---|---|---|---|
| 2026-01-20 | 0001822565-2026-00204 | Injury | Available | exact di |
| 2025-12-16 | 0001822565-2025-04531 | Injury | Available | exact di |
| 2025-11-17 | 0001825034-2025-03644 | Injury | Available | exact di |
| 2025-11-06 | 0001822565-2025-04025 | Injury | Available | exact di |
| 2025-11-03 | 0001822565-2025-03951 | Malfunction | Available | exact di |
| 2025-08-18 | 0001822565-2025-02994 | Injury | Available | exact di |
| 2024-12-11 | 0001822565-2024-03913 | Malfunction | Available | exact di |
| 2024-10-04 | 0001822565-2024-03185 | Injury | Available | exact di |
| 2023-05-11 | 0001822565-2023-01227 | Injury | Available | exact di |
| 2023-02-20 | 0001822565-2023-00447 | Malfunction | Available | exact di |
| 2023-01-13 | 0001822565-2023-00133 | Injury | Available | exact di |
| 2022-10-26 | 0001822565-2022-03001 | Malfunction | Available | exact di |
| 2022-06-06 | 14605118 | Injury | Available | catalog number |
| 2022-02-08 | 0001822565-2022-00379 | Injury | Available | exact di |
| 2021-08-24 | 0001822565-2021-02347 | Injury | Available | exact di |
Showing the most recent 16 of 18 linked reports.
Showing 1–15 of 16
Regulatory clearances
Predicate lineage
- K190656
Cited as predicate by: K210653
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 |
|---|---|---|---|---|
| 2022-07-27 | NAI | No action indicated | Zimmer, Inc. | 0 |
| 2022-07-27 | NAI | No action indicated | Zimmer, Inc. | 0 |
| 2020-10-01 | NAI | No action indicated | Zimmer Manufacturing B.V. | 0 |
| 2017-10-16 | VAI | Voluntary action indicated | Zimmer, Inc. | 8 |
| 2017-10-16 | VAI | Voluntary action indicated | Zimmer, Inc. | 8 |
| 2017-09-01 | NAI | No action indicated | Zimmer Trabecular Metal Technology, Inc. | 0 |
| 2017-07-27 | VAI | Voluntary action indicated | ZIMMER ORTHOPEDIC MFG LTD | 3 |
| 2017-07-20 | VAI | Voluntary action indicated | Zimmer Manufacturing B.V. | 3 |
| 2016-05-27 | WL | Warning Letter | Orthosoft, Inc. | — |
| 2016-05-23 | VAI | Voluntary action indicated | Zimmer Surgical Inc | 4 |
| 2015-11-20 | OAI | Official action indicated | Zimmer, Inc. | 10 |
| 2015-11-20 | OAI | Official action indicated | Zimmer, Inc. | 10 |
| 2015-11-17 | VAI | Voluntary action indicated | Zimmer Manufacturing B.V. | 4 |
| 2015-05-11 | VAI | Voluntary action indicated | Zimmer Trabecular Metal Technology, Inc. | 3 |
| 2014-10-16 | VAI | Voluntary action indicated | ZIMMER ORTHOPEDIC MFG LTD | 2 |
| 2014-06-11 | OAI | Official action indicated | Zimmer Manufacturing B.V. | 9 |
| 2014-05-28 | OAI | Official action indicated | Zimmer, Inc. | 12 |
| 2014-05-28 | OAI | Official action indicated | Zimmer, Inc. | 12 |
| 2014-02-07 | VAI | Voluntary action indicated | Zimmer, Inc. | 2 |
| 2014-02-07 | VAI | Voluntary action indicated | Zimmer, Inc. | 2 |
| 2013-08-19 | OAI | Official action indicated | Zimmer, Inc. | 0 |
| 2012-09-19 | WL | Warning Letter | Zimmer Manufacturing B.V. | — |
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