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

Class 2 Device Recall Centurion

  • 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 Centurion see related information
Date Initiated by Firm February 23, 2024
Date Posted March 29, 2024
Recall Status1 Open3, Classified
Recall Number Z-1434-2024
Recall Event ID 94136
Product Classification Retractor - Product Code GAD
Product Centurion retractor kits labeled as:
a) STERILE 6-1/2" SENN RETRACTOR (ST7185), Product Code 66795;
b) STERILE RAGNELL RETRACTOR (RR602), Product Code 67525;
c) ST. SENN RETRACTOR 3 PRG BLUNT (ST7085), Product Code 37535
Code Information a) 66795, UDI/DI 50653160061180 (case) 00653160061185 (each), Lot Numbers: 2023030190, 2023052390, 2023092590; b) 67525, UDI/DI 10653160158639 (case) 00653160158632 (ease), Lot Numbers: 2023032490; c) 37535, UDI/DI 10653160169048 (case) 00653160169041 (each), Lot Numbers: 2023061490
Recalling Firm/
3 Lakes Dr
Northfield IL 60093-2753
For Additional Information Contact Karin Johnson
Manufacturer Reason
for Recall
Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users.
FDA Determined
Cause 2
Process control
Action Medline Industries, LP, issued a Medical Device Recall notice to its consignees on 02/27/2024 via email and USPS First Class mail. The notice explained the problem with the devices, risk, and requested that the products be destroyed at the consignee. Distributors were directed to notify their customers.
Quantity in Commerce 760 units
Distribution Worldwide distribution - US Nationwide and the countries of Panama, Canada.
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.