CAPSUREFIX NOVUS LEAD MRI SURESCAN
Report
- Report Number
- 2649622-2026-15094
- Event Type
- Injury
- Date Received
- May 21, 2026
- Date of Event
- April 22, 2026
- Report Date
- May 21, 2026
- Manufacturer
- MEDTRONIC PUERTO RICO VILLALBA
- Product Code
- DTB
- UDI-DI
- 00643169550766
- PMA / PMN Number
- P930039
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
CONTINUATION OF D10: 0155 LEAD IMPLANTED: (B)(6) 2001 MEDTRONIC SUBMITS THIS REPORT TO COMPLY WITH FDA REGULATIONS 21 CFR PARTS 4 AND 803. MEDTRONIC HAS MADE REASONABLE EFFORTS TO PROVIDE AS MUCH RELEVANT INFORMATION AS IS AVAILABLE TO THE COMPANY AS OF THE SUBMISSION DATE OF THIS REPORT. THIS REPORT DOES NOT CONSTITUTE AN ADMISSION OR A CONCLUSION BY FDA, MEDTRONIC, OR ITS EMPLOYEES THAT THE DEVICE, MEDTRONIC, OR ITS EMPLOYEE CAUSED OR CONTRIBUTED TO THE EVENT DESCRIBED IN THE REPORT. ANY REQUIRED FIELDS THAT ARE UNPOPULATED ARE BLANK BECAUSE THE INFORMATION IS CURRENTLY UNKNOWN OR UNAVAILABLE. MEDTRONIC WILL SUBMIT A SUPPLEMENTAL REPORT IF ADDITIONAL RELEVANT INFORMATION BECOMES KNOWN.
IT WAS REPORTED THAT APPROXIMATELY ONE MONTH POST IMPLANT THE PATIENT EXPERIENCED A POCKET INFECTION WITH DISCOMFORT, PURULENT DISCHARGE/PUS, REDNESS, SWELLING, AND WOUND DEHISCENCE. THE LEADS WERE CUT, AND THE ICD WAS REMOVED. A LEADLESS IMPLANTABLE PULSE GENERATOR (IPG) WAS IMPLANTED. NO FURTHER PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 241142 | CAPSUREFIX NOVUS LEAD MRI SURESCAN | PERMANENT PACEMAKER ELECTRODE | DTB | MEDTRONIC PUERTO RICO VILLALBA | 5076-52 | 00643169550766 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 91 YR | Male | Hospitalization| R | DDPA2D1 ICD |