FDA Adverse Event Injury Summary report: N

PERCEPTA QUAD CRT-P MRI SURESCAN

MDR report key: 24699003 · Received March 26, 2026

Report

Report Number
9614453-2026-01160
Event Type
Injury
Date Received
March 26, 2026
Date of Event
January 21, 2024
Report Date
March 26, 2026
Manufacturer
MEDTRONIC EUROPE SARL
Product Code
NKE
UDI-DI
00643169891418
PMA / PMN Number
P010015
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

H11: THIS REGULATORY REPORT IS BEING SUBMITTED AS PART OF A RETROSPECTIVE REVIEW AND REMEDIATION RELATED TO CAPA 711948. CONTINUATION OF D10: 429878 IMPLANTED: (B)(6) 2023, TYRX-AAE IMPLANTED: (B)(6) 2023, 350 974 LEAD IMPLANTED: (B)(6) 2013, 350 973 LEAD IMPLANTED: (B)(6) 2013. 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.

Description of Event or Problem · 0

IT WAS REPORTED THAT APPROXIMATELY ONE MONTH POST IMPLANT OF A CARDIAC RESYNCHRONIZATION THERAPY PACEMAKER (CRT-P) SYSTEM WITH AN ANTIBACTERIAL ABSORBABLE ENVELOPE, THE PATIENT PRESENTED WITH AN INFECTION. THE CRTP SYSTEM WAS EXPLANTED AND REPLACED. NO FURTHER PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
760390 PERCEPTA QUAD CRT-P MRI SURESCAN PULSE GENERATOR, PACEMAKER, IMPLANTABLE, WITH CARDIAC RESYNCHRONIZATION (CRT-P) NKE MEDTRONIC EUROPE SARL W4TR01 00643169891418

Patients

Seq Age Sex Outcome Treatment
1 78 YR Male Required Intervention| H "SEE H11...."