FDA Adverse Event Injury Summary report: N

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

MDR report key: 11562481 · Received March 24, 2021

Report

Report Number
2024168-2021-02330
Event Type
Injury
Date Received
March 24, 2021
Date of Event
March 2, 2021
Report Date
March 24, 2021
Manufacturer
ABBOTT VASCULAR
Product Code
MGB
UDI-DI
08717648013089
PMA / PMN Number
P960043
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE WAS NOT RETURNED FOR ANALYSIS. A REVIEW OF THE LOT HISTORY RECORD IDENTIFIED NO MANUFACTURING NONCONFORMITIES ISSUED TO THE REPORTED LOT THAT WOULD HAVE CONTRIBUTED TO THIS EVENT. THE REPORTED DIFFICULTIES AND SUBSEQUENT TREATMENT APPEAR TO BE RELATED TO AN INTERACTION OF THE DEVICE WITH PATIENT ANATOMY OR INABILITY TO MAINTAIN POSITION/STABILITY OF THE DEVICE DURING DEPLOYMENT DUE TO CIRCUMSTANCES OF THE PROCEDURE. THERE IS NO INDICATION OF A PRODUCT QUALITY ISSUE WITH RESPECT TO MANUFACTURE, DESIGN OR LABELING. THE ADDITIONAL PROGLIDE DEVICE REFERENCED IS FILED UNDER SEPARATE MEDWATCH REPORT NUMBER.

Description of Event or Problem · 1

IT WAS REPORTED THAT SUTURE PLACEMENT IN THE LEFT COMMON FEMORAL VEIN WAS ATTEMPTED WITH TWO PROGLIDE DEVICES USING THE PRE-CLOSE TECHNIQUE VIA A 6F SHEATH PRIOR TO AN ELECTROPHYSIOLOGY INTERVENTIONAL PROCEDURE. REPORTEDLY, NO SUTURE WAS PRESENT WHEN THE PLUNGER OF BOTH PROGLIDE DEVICES WAS REMOVED. THE SHEATH WAS UPSIZED TO A 9F AND THE ELECTROPHYSIOLOGY PROCEDURE WAS COMPLETED. A NON-ABBOTT DEVICE WAS USED TO ACHIEVE HEMOSTASIS. THERE WAS NO REPORTED ADVERSE PATIENT SEQUELA AND NO REPORTED CLINICALLY SIGNIFICANT DELAY IN THE PROCEDURE OR THERAPY. NO ADDITIONAL INFORMATION WAS PREOVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
460051 PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM SUTURE MEDIATED CLOSURE MGB ABBOTT VASCULAR 12673-03 0120741 08717648013089

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention 6F SHEATH