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

Class 2 Device Recall Cordis SABER PTA Balloon Dilation Catheter

  • 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 Cordis SABER PTA Balloon Dilation Catheter see related information
Date Initiated by Firm July 19, 2021
Create Date August 09, 2021
Recall Status1 Open3, Classified
Recall Number Z-2235-2021
Recall Event ID 88348
510(K)Number K133843  
Product Classification Catheter, angioplasty, peripheral, transluminal - Product Code LIT
Product Cordis SABER PTA Balloon Dilation Catheter, 4F, REF 48004010X
Code Information Lot/Batch number 82219442
Recalling Firm/
Manufacturer
Cordis Corporation
14201 NW 60th Ave
Miami Lakes FL 33014-2802
For Additional Information Contact
786-313-2000
Manufacturer Reason
for Recall
The balloon protective sheath may potentially be contaminated with a foreign material left over from the manufacturing process. The contaminant may transfer over from the sheath to the balloon.
FDA Determined
Cause 2
Under Investigation by firm
Action The firm initiated the recall by letter on 07/19/2021. The letter explained the issue and requested the return of the devices.
Quantity in Commerce 8 units
Distribution Worldwide distribution - US Nationwide distribution in the states of CA, OH, and the countries of Switzerland, Portugal, and Poland.
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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database 510(K)s with Product Code = LIT and Original Applicant = CORDIS CORPORATION
-
-