• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall VascuTape Radiopaque Tape

  • Print
  • Share
  • E-mail
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC

New Search Back to Search Results
  Class 2 Device Recall VascuTape Radiopaque Tape see related information
Date Initiated by Firm March 18, 2013
Date Posted April 04, 2013
Recall Status1 Terminated 3 on December 03, 2014
Recall Number Z-1055-2013
Recall Event ID 64704
510(K)Number K932184  
Product Classification Assembly, thigh/knee/shank/ankle/foot, external - Product Code KFX
Product Glow 'N Tell 20 cm Tape: 1100-00 (100 strips); 1100-50 (50 strips); 1100-20 (20 strips).

Intended to be placed on the skin to assist during imaging procedures.
Code Information SGL1190, exp 2017-02; SGL1196, exp 2017-09; SGL1197, exp. 2017-09
Recalling Firm/
LeMaitre Vascular, Inc.
63 2nd Ave
Burlington MA 01803-4413
For Additional Information Contact Laurie Churchill
781-221-2266 Ext. 108
Manufacturer Reason
for Recall
Devices were not sealed correctly during the manufacturing process, and the sterility of these products have been compromised.
FDA Determined
Cause 2
Packaging process control
Action LeMaitre sent an "URGENT:VASCUTAPE RADIOPAQUE TAPE DEVICE FIELD SAFETY NOTICE" dated March 20, 2013 to affected customers. The recall letter contains a form that requests customers to return to LeMaitre Vascular, Inc. as a record of notification and reconciliation. The letter provides instructions on how the customer can inspect the defective tape seals and/or return the affected products for replacement/credit.
Quantity in Commerce 13560
Distribution Worldwide Distribution-USA (nationwide) and the countries of Canada, EU, and Asia.
Total Product Life Cycle TPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = KFX and Original Applicant = VASCUTECH, INC.