InjuryMMX
AVEIR¿ RETRIEVAL SYSTEM CATHETER
Received Aug 21, 2024 · Event occurred Nov 16, 2023
Report 2017865-2024-62860 · MDR key 20013410
Device
Generic name
Device, Percutaneous Retrieval
Manufacturer
St. Jude Medical, Inc.(crm-sylmar)Model number
LSCR111Product problems
- Adverse Event Without Identified Device or Use Problem
- Adverse Event Without Identified Device or Use Problem
Patient
73 YR · Male
- Unspecified Infection
- Unspecified Infection
Narrative
Additional Manufacturer Narrative
REVIEW OF STERILIZATION RECORDS UNABLE TO BE COMPLETED AS THERE WAS NO IDENTIFYING PRODUCT INFORMATION.
Description of Event or Problem
IT WAS REPORTED THROUGH HEART RHYTHM CASE REPORTS THAT FIVE DAYS POSTRETRIEVAL, THE RIGHT FEMORAL SURGICAL SITE DEVELOPED AN INFECTION. IT WAS SUCCESSFULLY TREATED WITH ANTIBIOTICS AND DRAINAGE. THE PATIENT WAS STABLE.