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U.S. Department of Health and Human Services

Class 2 Device Recall daVinci

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 Class 2 Device Recall daVincisee related information
Date Initiated by FirmJanuary 24, 2013
Date PostedMay 29, 2013
Recall Status1 Terminated 3 on May 30, 2013
Recall NumberZ-1424-2013
Recall Event ID 65094
510(K)NumberK090993 
Product Classification System,surgical,computer controlled instrument - Product Code NAY
ProductUser Manual addendum, TORS for da Vinci Surgical System IS 1200, IS 2000 and IS 3000. Product Usage: The user manual for Transoral Surgery (TORS) provided information to update and replace the Indications for Use and Representative uses section and add the section Warnings for Transoral Otolaryngology Surgery.
Code Information Model number 552002-01
Recalling Firm/
Manufacturer		 Intuitive Surgical, Inc.
1266 Kifer Rd Bldg 100
Sunnyvale CA 94086-5304
For Additional Information ContactRichard Reeves
408-523-2244
Manufacturer Reason
for Recall		Change to User Manual to remove one indication for use and amend warnings to emphasize restrictions for use.
FDA Determined
Cause 2		Labeling False and Misleading
ActionIntuitive sent an Important Medical Device Correction letters dated January 24, 2013 via Federal Express to all affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to locate and discard the existing TORS addendum, place the new TORS addendum included with this letter with your System User Manual, and complete and return the attached Acknowledgement Form to Intuitive Surgical. For questions call Intuitive Surgical Customer Service at 1-800-876-1310.
Quantity in Commerce1,374
DistributionUS Distribution Only
Total Product Life CycleTPLC 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) Database510(K)s with Product Code = NAY
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