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

Class 2 Device Recall Starion Instruments Real Hand ThermaSeal Thermal Ligating Shears

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC | Inspections
 


New Search Back to Search Results
 Class 2 Recall
Starion Instruments Real Hand ThermaSeal Thermal Ligating Shears
see related information
Date Posted July 09, 2010
Recall Status1 Terminated on October 27, 2010
Recall Number Z-1972-2010
Recall Event ID 55750
Premarket Notification
510(K) Number
K062257 
Product Classification Electrosurgical, Cutting & Coagulation & Accessories - Product Code GEI
Product Starion Instruments Real Hand ThermaSeal Thermal Ligating Shears, electrosurgical cutting and coagulation device and accessories, manufactured by Starion Instruments, Sunnyvale, CA Intended use: Medical Device used for cutting and cauterization of soft tissue during surgery, and of natural or synthetic, non-metallic sutures during surgery.
Code Information Model Number N-10700, lot numbers 80419, 806009, 804037, 804035, 804036, 804019A.
Recalling Firm/
Manufacturer
Starion Instruments
775 Palomar Ave
Sunnyvale, California 94085-2915
Consumer Instructions Contact the recalling firm for information
Manufacturer Reason
for Recall
Due to an improper fixture revision, device may be missing a screw at the jaw assembly, resulting in jaw components falling off during use.
FDA Determined
Cause 2
PRODUCTION CONTROLS: Process Control
Action The firm submitted an MDR but determined that there was no risk to health. E-mails were sent on June 26, 2008, to consignees, describing the product, the problem, and action to be taken by consignees. The consignees were ask to provide a list of all unused ThermaSeal devices and their locations, to return the products to Starion from the lots noted and to provide a copy of the attached letter to their sales force and customers if they choose. If you have any questions, please call (408) 522-5200 ext. 326 or (408) 350-9934.
Quantity in Commerce 217 units
Distribution Worldwide distribution.
Total Product Life Cycle TPLC Device Report

 
1 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
510(K) Database 510(K)s with Product Code = GEI and Original Applicant = STARION INSTRUMENTS
-
-