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 JustRight 5mm Reload

  • 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 JustRight 5mm Reload see related information
Date Initiated by Firm August 27, 2014
Date Posted September 23, 2014
Recall Status1 Terminated 3 on October 06, 2014
Recall Number Z-2691-2014
Recall Event ID 69140
510(K)Number K132472  
Product Classification Staple, implantable - Product Code GDW
Product Justright Surgical, JustRight 5mm Reload, REFJR-REL25-2.0, Sterile, EO, Rx Only

It is a replacement cartridge used when more than one firing is required during a surgery.
Code Information Lot: 75FD0417
Recalling Firm/
Manufacturer		 Justright Surgical, LLC
6325 Gunpark Dr
Suite G
Boulder CO 80301-3592
For Additional Information Contact Claire C. Bronstein
720-287-7146
Manufacturer Reason
for Recall		 JustRight Surgical is recalling specific lots of JustRight 5mm Stapler and Reload products because they may deliver poor distal staple formation, past the end of the knife cut.
FDA Determined
Cause 2		 Process design
Action Consignees were notified via letter on August 27, 2014 in addition, the sales rep will hand deliver the Recall Notification on 8/28/14. Acknowledgement Form will be provided and returned products will be sent to STD Med where it will be held in quarantine.
Quantity in Commerce 3 cases containing 36 units
Distribution Distributed in the states of Colorado, California and New York.
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 = GDW and Original Applicant = JUSTRIGHT SURGICAL, LLC
-
-