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

Class 2 Device Recall Straight Esthetic 4.0 mm 1mm Cuff Abutment

  • 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 Straight Esthetic 4.0 mm 1mm Cuff Abutment see related information
Date Initiated by Firm July 05, 2011
Date Posted March 08, 2013
Recall Status1 Terminated 3 on March 11, 2013
Recall Number Z-0923-2013
Recall Event ID 64477
510(K)Number K101545  
Product Classification Abutment, implant, dental, endosseous - Product Code NHA
Product Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment
Part Number: G71200

Genesis implant for single stage or two stage surgical procedures all types of of bone in partially or fully edentulous mandibles and maxillae.
Code Information Lot Number: 2376 Exp Date: 09/2013
Recalling Firm/
Keystone Dental Inc
144 Middlesex Tpke
Burlington MA 01803-4403
For Additional Information Contact SAME
Manufacturer Reason
for Recall
Mislabeled: Genesis Straight Esthetic 5.0mm Contour ,3mm cuff labeled as Genesis Straight Esthetic 4.0 mm, 1 mm cuff abutment,
FDA Determined
Cause 2
Mixed-up of materials/components
Action Keystone issued Market Withdrawal notice via fax on July 5, 2011, to affected customers. The notice identified the product, the problem, and the action to be taken by the customer. Customers were asked to complete and return the fax-back form to facilitate whether they hae any affected product and indicate whether they would like to receive a replacement of a full refund. Customers ewre asked to contact Keyston'es Customer Relations Department to coordinate shipment of the returned product. For questions regarding this recall call 781-328-3390.
Quantity in Commerce 35 units
Distribution Nationwide Distribution including CA, IN, MA, MD, MN, MI, , NH, NY, NC, PA, and WI.
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 = NHA and Original Applicant = KEYSTONE DENTAL