Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall Ponsky PEG

  • 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 Ponsky PEG see related information
Date Initiated by Firm December 04, 2008
Date Posted September 15, 2009
Recall Status1 Terminated 3 on November 09, 2011
Recall Number Z-2181-2009
Recall Event ID 50678
510(K)Number K061021  K915841  K972101  K972025  K033562  
Product Classification Polypectomy snare for Percutaneous Endoscopic Gastrostomy - Product Code KNT
Product Bard Access Systems, Inc., Ponsky* PEG (Percutaneous Endoscopic Gastrostomy) Safety System - "Pull" REF 003025, 16F, Sterile.
Code Information Lots: HURF0569, HURK1559, HUSA1491, HUSF1992,  HUSJ0248
Recalling Firm/
Manufacturer		 C.R. Bard Access Systems, Inc
5425 Amelia Earhart Dr
Salt Lake City UT 84116-3713
For Additional Information Contact
801-595-0700
Manufacturer Reason
for Recall		 Snare can detach in patient. The Polypectomy Snares and the Entake Peg System (which contain these snares) are being recalled because the looped portion of the snare can become detached and drop into the stomach or other internal canal during use, necessitating retrieval of the remaining piece.
FDA Determined
Cause 2		 Nonconforming Material/Component
Action Bard contacted all 1,883 worldwide customers who received the distributed suspect 467 product code lots, comprising 177, 614 units that were either not expired or were still available in the field. These will be returned by the customer to Bard Access Systems. 1-800-290-1689.
Quantity in Commerce 177,614 units
Distribution Worldwide, including USA, Belgium, Canada, Australia, and Japan.
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 = KNT and Original Applicant = C.R. BARD, INC.
510(K)s with Product Code = KNT and Original Applicant = CONMED CORP.
510(K)s with Product Code = KNT and Original Applicant = HERAEUS KULZER, INC.
510(K)s with Product Code = KNT and Original Applicant = RADIUS INTL., INC.
-
-