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.
1 linked reportMalfunction 1
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2019-01 | 0 | 1 |
| 2019-02 | 0 | 2 |
| 2019-03 | 0 | 2 |
| 2019-04 | 0 | 3 |
| 2019-05 | 0 | 1 |
| 2019-06 | 0 | 2 |
| 2019-07 | 0 | 1.67 |
| 2019-08 | 0 | 1.5 |
| 2019-09 | 0 | 1.5 |
| 2019-10 | 0 | 1 |
| 2019-12 | 0 | 3.5 |
| 2020-01 | 0 | 1.33 |
| 2020-02 | 0 | 1 |
| 2020-03 | 0 | 1 |
| 2020-04 | 0 | 1.67 |
| 2020-06 | 0 | 2 |
| 2020-08 | 0 | 1.5 |
| 2020-09 | 0 | 1.5 |
| 2020-10 | 0 | 2 |
| 2020-12 | 0 | 2.25 |
| 2021-01 | 0 | 2.75 |
| 2021-02 | 0 | 1.67 |
| 2021-03 | 0 | 1.67 |
| 2021-04 | 0 | 2 |
| 2021-05 | 0 | 1.29 |
| 2021-06 | 0 | 1.5 |
| 2021-07 | 0 | 2 |
| 2021-08 | 0 | 1.25 |
| 2021-09 | 0 | 1 |
| 2021-10 | 0 | 2 |
| 2021-11 | 0 | 2 |
| 2021-12 | 0 | 1.33 |
| 2022-01 | 0 | 2 |
| 2022-02 | 0 | 3 |
| 2022-03 | 0 | 2 |
| 2022-04 | 0 | 1.5 |
| 2022-05 | 0 | 1.75 |
| 2022-06 | 0 | 1.38 |
| 2022-07 | 0 | 6 |
| 2022-09 | 0 | 1 |
| 2022-10 | 0 | 2 |
| 2022-11 | 0 | 3.5 |
| 2022-12 | 0 | 2 |
| 2023-01 | 0 | 2.33 |
| 2023-02 | 0 | 1.5 |
| 2023-03 | 0 | 2.25 |
| 2023-04 | 1 | 1.82 |
| 2023-05 | 0 | 1.8 |
| 2023-06 | 0 | 4.43 |
| 2023-07 | 0 | 2.75 |
| 2023-08 | 0 | 1.86 |
| 2023-09 | 0 | 2.67 |
| 2023-10 | 0 | 2.33 |
| 2023-11 | 0 | 2.33 |
| 2023-12 | 0 | 2.67 |
| 2024-01 | 0 | 3.5 |
| 2024-02 | 0 | 2.25 |
| 2024-03 | 0 | 3 |
| 2024-04 | 0 | 5.4 |
| 2024-05 | 0 | 2.6 |
| 2024-06 | 0 | 1.14 |
| 2024-07 | 0 | 2 |
| 2024-08 | 0 | 2.14 |
| 2024-09 | 0 | 3.25 |
| 2024-10 | 0 | 4.5 |
| 2024-11 | 0 | 3.75 |
| 2024-12 | 0 | 2.33 |
| 2025-01 | 0 | 3.8 |
| 2025-02 | 0 | 5 |
| 2025-03 | 0 | 2.56 |
| 2025-04 | 0 | 2 |
| 2025-05 | 0 | 2.83 |
| 2025-06 | 0 | 2.67 |
| 2025-07 | 0 | 3 |
| 2025-08 | 0 | 3.5 |
| 2025-09 | 0 | 1.67 |
| 2025-10 | 0 | 1.33 |
| 2025-11 | 0 | 2.73 |
| 2025-12 | 0 | 4.25 |
| 2026-01 | 0 | 1 |
| 2026-02 | 0 | 2.95 |
| 2026-03 | 0 | 2.2 |
| 2026-04 | 0 | 2.59 |
| 2026-05 | 0 | 2.28 |
| 2026-06 | 0 | 4.23 |
Failure-mode summaryAI-generated
1 linked report narrative available — no AI summary generated yet.
Recall history
| Initiated | Recall # | Class | Status | Reason | Quantity | Link basis |
|---|---|---|---|---|---|---|
| 2022-08-12 | Z-0182-2023 | Class II | Open, Classified | Due to un-commanded movement of mobile x-ray unit.Distribution: U.S.: KY, WI, FL, DE, WV, CA, MO, NY, NC, AL, AR, MS, GA, IL, IA, TN, KS, KY, IN, HI, OH, WY, PA, NV, RI, UT, AZ, OK, MN, ME, MT, WA, VA, SD, MI, LA, and TX O.U.S.: N/A | 155 systems | code info di |
Individual MAUDE reports
| Date | Report # | Type | Narrative | Link basis |
|---|---|---|---|---|
| 2023-04-27 | 9617251-2023-00003 | Malfunction | Available | model number |
Regulatory clearances
- 510(k)K192936Substantially equivalent (SESE) · 2019-11-15clearance family
Predicate lineage
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 |
|---|---|---|---|---|
| 2025-01-24 | OAI | Official action indicated | SEDECAL SA | 4 |
| 2013-06-28 | VAI | Voluntary action indicated | SEDECAL SA | 2 |
| 2010-01-15 | NAI | No action indicated | SEDECAL SA | 0 |
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