FDA Enforcement Class II Terminated

Percuvance(R) Percutaneous Shaft 29cm, PCVSH3 The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate Intended Use: soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips to soft tissue during laparoscopic surgery.

Recall: Z-0753-2019 · Reported January 30, 2019

Enforcement

Recall Number
Z-0753-2019
Event ID
81909
Classification
Class II
Status
Terminated
Product Type
Devices
Firm
Teleflex Medical
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
January 30, 2019
Initiation Date
January 3, 2018
Classification Date
January 18, 2019
Termination Date
October 30, 2020
Address
3015 Carrington Mill Blvd, N/A, Morrisville, NC, 27560-5437, United States

Description

Percuvance(R) Percutaneous Shaft 29cm, PCVSH3 The Percutaneous Surgical System with 5mm attachments is indicated for the means to penetrate Intended Use: soft tissue to access certain areas of the abdomen. The system is used to grasp, manipulate, cut, cauterize and deliver Hem-o-lok ligating clips to soft tissue during laparoscopic surgery.

Reason

There is potential for a piece of the distal tip on the Percuvance shaft to become deformed and possibly break off during use. If a piece did break off it could compromise the functionality and security of the tool tip. Should this occur during use, surgical intervention may be required.

Code Info

Batch/Lot Numbers: 73A1700531, 73B1700180, 73F1700583, 73F1700584, 73F1700585, 73H1700728, 73J1600394, 73J1700072, 73J1700073, 73J1700074, 73J1700554

Distribution

Worldwide Distribution: US (nationwide) and countries of: Australia, Belgium, China, Czech Republic, France, Germany, Great Britain, Iran, Ireland, Italy, Japan, Lebanon, Netherlands, Qatar, Romania, Saudi Arabia, Singapore, Spain, Taiwan, Turkey, and the United Arab Emirates.

Quantity

1751 units