FDA Adverse Event
Injury
Summary report: N
AXONICS
MDR report key: 22155114
·
Received June 5, 2025
Report
- Report Number
- 2124215-2025-35173
- Event Type
- Injury
- Date Received
- June 5, 2025
- Date of Event
- May 9, 2025
- Report Date
- June 23, 2025
- Manufacturer
- AXONICS MODULATION TECHNOLOGIES, INC.
- Product Code
- EZW
- UDI-DI
- 10810005340455
- PMA / PMN Number
- P180046
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
Additional Manufacturer Narrative · 0
CORRECTION TO SECTION H6 PATIENT CODES: PAIN CODE UPDATED TO IMPLANT PAIN CODE. ADDITIONAL PRODUCT CODE: QON ADDITIONAL PREMARKET/510K: P190006.
Additional Manufacturer Narrative · 0
ADDITIONAL PRODUCT CODE: QON ADDITIONAL PREMARKET/510K: P190006.
Description of Event or Problem · 0
IT WAS REPORTED THAT THIS NEUROSTIMULATOR MIGRATED, CAUSING PAIN. A DEVICE REVISION WAS PERFORMED AND THE DEVICE WAS MOVED TO THE OTHER SIDE OF THE PATIENT. THERE WERE NO ADDITIONAL PATIENT COMPLICATIONS.
Description of Event or Problem · 0
IT WAS REPORTED THAT THIS NEUROSTIMULATOR MIGRATED, CAUSING PAIN. A DEVICE REVISION WAS PERFORMED AND THE DEVICE WAS MOVED TO THE OTHER SIDE OF THE PATIENT. THERE WERE NO ADDITIONAL PATIENT COMPLICATIONS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 551523 | AXONICS | STIMULATOR, ELECTRICAL, IMPLANTABLE, FOR INCONTINENCE | EZW | AXONICS MODULATION TECHNOLOGIES, INC. | 4101 | AX1T054475 | 10810005340455 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 58 YR | Female | Required Intervention| H |