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 Endotec TMJ Components

  • 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 Endotec TMJ Components see related information
Date Initiated by Firm June 05, 2009
Date Posted May 20, 2010
Recall Status1 Terminated 3 on October 22, 2013
Recall Number Z-1626-2010
Recall Event ID 52527
Product Classification TMJ Components - Product Code JWH
Product TMJ Components:

Right Ramus Component - DelCristo Catalog: 09-11-0215,
TMJ - Shah Catalog: 09-42-0217, 09-11-0217.
Left Fossa Component - DelCristo Catalog 09-42-0216,
Left Ramus Component - DelCristo Catalog: 09-11-0216.
Code Information Lot No: 09110215NN373 09110216NN373 09110217NN379 09420216NN373 09520217NN379 
Recalling Firm/
Manufacturer		 Endotec, Inc.
2546 Hansrob Rd
Orlando FL 32804-3318
For Additional Information Contact
407-822-0021
Manufacturer Reason
for Recall		 Endotec is recalling B-P Hip, B-P Shoulder, and B-P Knee Replacement System devices due to sterility issues involving validation, process variations and test results.
FDA Determined
Cause 2		 Other
Action Recall Letters were sent to each distributor on 06/07/2009. Questions are directed to Endotec at (407) 822-0021.
Quantity in Commerce 5 Pieces
Distribution Worldwide distribution -- US in OH, TX, CA, FL, NJ, TN; and International Distribution: Korea, Australia, Switzerland, The Netherlands, Spain. Domestic: OH, TX, CA, FL, NJ, TN.
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.
-
-