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.
19 linked reportsMalfunction 13Injury 6
| Month | This device (reports) | Product-code average (reports per device) |
|---|---|---|
| 2019-01 | 0 | 1.5 |
| 2019-02 | 0 | 1 |
| 2019-03 | 0 | 2.75 |
| 2019-04 | 0 | 3 |
| 2019-05 | 0 | 2.67 |
| 2019-06 | 0 | 2 |
| 2019-07 | 0 | 2.88 |
| 2019-08 | 0 | 2.25 |
| 2019-09 | 0 | 2.83 |
| 2019-10 | 0 | 2 |
| 2019-11 | 0 | 2.67 |
| 2019-12 | 0 | 3 |
| 2020-01 | 0 | 3.25 |
| 2020-02 | 0 | 3.5 |
| 2020-03 | 0 | 2.67 |
| 2020-04 | 0 | 2.25 |
| 2020-05 | 0 | 2 |
| 2020-06 | 0 | 2.2 |
| 2020-07 | 0 | 4.5 |
| 2020-08 | 1 | 3 |
| 2020-09 | 0 | 3.25 |
| 2020-10 | 0 | 3 |
| 2020-11 | 0 | 2.44 |
| 2020-12 | 0 | 3 |
| 2021-01 | 0 | 3 |
| 2021-02 | 0 | 5 |
| 2021-03 | 0 | 4.33 |
| 2021-04 | 0 | 3.14 |
| 2021-05 | 0 | 2.6 |
| 2021-06 | 0 | 3.6 |
| 2021-07 | 0 | 4 |
| 2021-08 | 0 | 2.6 |
| 2021-09 | 0 | 2.5 |
| 2021-10 | 0 | 4 |
| 2021-11 | 0 | 3 |
| 2021-12 | 0 | 2.2 |
| 2022-01 | 0 | 3 |
| 2022-02 | 0 | 2.82 |
| 2022-03 | 0 | 6 |
| 2022-04 | 0 | 3 |
| 2022-05 | 0 | 3.5 |
| 2022-06 | 0 | 2.78 |
| 2022-07 | 0 | 3.17 |
| 2022-08 | 0 | 3.67 |
| 2022-09 | 0 | 3.8 |
| 2022-10 | 0 | 2.67 |
| 2022-11 | 0 | 3.2 |
| 2022-12 | 0 | 3 |
| 2023-01 | 0 | 4 |
| 2023-02 | 0 | 2.6 |
| 2023-03 | 0 | 2.6 |
| 2023-04 | 0 | 4 |
| 2023-05 | 0 | 2.29 |
| 2023-06 | 0 | 2.75 |
| 2023-07 | 0 | 2.29 |
| 2023-08 | 0 | 2.6 |
| 2023-09 | 0 | 2.29 |
| 2023-10 | 0 | 4.25 |
| 2023-11 | 0 | 4.4 |
| 2023-12 | 0 | 2.25 |
| 2024-01 | 0 | 1.33 |
| 2024-02 | 0 | 3 |
| 2024-03 | 0 | 2.75 |
| 2024-04 | 0 | 3.5 |
| 2024-05 | 0 | 3.42 |
| 2024-06 | 0 | 3.4 |
| 2024-07 | 0 | 2.5 |
| 2024-08 | 0 | 3 |
| 2024-09 | 0 | 2.75 |
| 2024-10 | 0 | 1.67 |
| 2024-11 | 0 | 4.27 |
| 2024-12 | 0 | 2.33 |
| 2025-01 | 0 | 2.08 |
| 2025-02 | 0 | 2.5 |
| 2025-03 | 0 | 2.22 |
| 2025-04 | 12 | 3.25 |
| 2025-05 | 0 | 3.13 |
| 2025-06 | 3 | 3.56 |
| 2025-07 | 3 | 4.21 |
| 2025-08 | 0 | 3.5 |
| 2025-09 | 0 | 3.54 |
| 2025-10 | 0 | 2.84 |
| 2025-11 | 0 | 2.89 |
| 2025-12 | 0 | 2.18 |
| 2026-01 | 0 | 3.68 |
| 2026-02 | 0 | 4 |
| 2026-03 | 0 | 2.53 |
| 2026-04 | 0 | 2.88 |
| 2026-05 | 0 | 2.84 |
| 2026-06 | 0 | 5.37 |
Failure-mode summaryAI-generated
19 linked report narratives available — no AI summary generated yet.
Recall history
| Initiated | Recall # | Class | Status | Reason | Quantity | Link basis |
|---|---|---|---|---|---|---|
| 2025-07-07 | Z-2273-2025 | Class I | Open, Classified | Certain batches are being removed due to an increase in complaints received in which physicians encountered greater than anticipated resistance while attempting to withdraw the stent delivery system (SDS) from the guidewire or embolic protection device (EPD) after successful stent deployment. The most serious potential adverse health consequence is stroke. Other risks include delay to procedure, vessel injury, vessel spasm, or stent disruption/damage necessitating additional intervention.Distribution: Domestic US Nationwide distribution including Puerto Rico. International distribution worldwide. | 26,570 (1,333 US; 25,174 OUS) | code info di |
Individual MAUDE reports
| Date | Report # | Type | Narrative | Link basis |
|---|---|---|---|---|
| 2025-07-09 | 2124215-2025-43644 | Malfunction | Available | catalog number |
| 2025-06-09 | 2124215-2025-36610 | Malfunction | Available | catalog number |
| 2025-04-29 | 2124215-2025-26689 | Injury | Available | catalog number |
| 2025-04-29 | 2124215-2025-23845 | Injury | Available | catalog number |
| 2025-04-11 | 2124215-2025-22171 | Malfunction | Available | catalog number |
| 2025-04-11 | 2124215-2025-22459 | Malfunction | Available | catalog number |
| 2020-08-03 | 2134265-2020-10334 | Malfunction | Available | exact di |
Showing the most recent 7 of 19 linked reports.
Regulatory clearances
- PMAP050019Approved (APPR) · 2025-09-19 · +19 earlier decisionsclearance family
Manufacturer compliance record
| Date | Type | Outcome | Facility | Citations |
|---|---|---|---|---|
| 2025-04-07 | OAI | Official action indicated | Boston Scientific Corporation | 9 |
| 2025-04-07 | OAI | Official action indicated | Boston Scientific Corporation | 9 |
| 2025-03-18 | NAI | No action indicated | Boston Scientific Corporation | 0 |
| 2025-03-18 | NAI | No action indicated | Boston Scientific Corporation | 0 |
| 2024-12-06 | NAI | No action indicated | Nalu Medical, Inc. | 0 |
| 2024-11-26 | VAI | Voluntary action indicated | Boston Scientific Corporation | 3 |
| 2024-11-26 | VAI | Voluntary action indicated | Boston Scientific Corporation | 3 |
| 2024-06-13 | NAI | No action indicated | Elutia Inc | 0 |
| 2024-01-23 | VAI | Voluntary action indicated | Silk Road Medical | 1 |
| 2023-12-05 | NAI | No action indicated | Valencia Technologies Corporation | 0 |
| 2023-12-01 | VAI | Voluntary action indicated | Corbin Clinical Resources, Llc | 1 |
| 2023-08-01 | NAI | No action indicated | Boston Scientific Corporation | 0 |
| 2023-08-01 | NAI | No action indicated | Boston Scientific Corporation | 0 |
| 2023-04-05 | NAI | No action indicated | Intera Oncology, Inc. | 0 |
| 2022-07-28 | NAI | No action indicated | Boston Scientific Corporation | 0 |
| 2022-07-28 | NAI | No action indicated | Boston Scientific Corporation | 0 |
| 2022-06-02 | VAI | Voluntary action indicated | Boston Scientific de Costa Rica SRL | 0 |
| 2022-03-23 | NAI | No action indicated | Axonics, Inc. | 0 |
| 2021-11-17 | VAI | Voluntary action indicated | Valencia Technologies Corporation | 1 |
| 2021-10-29 | NAI | No action indicated | Boston Scientific Corporation | 0 |
| 2014-04-10 | WL | Warning Letter | Boston Scientific Corporation | — |
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