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U.S. Department of Health and Human Services

Class 2 Device Recall Flush Port

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 Class 2 Device Recall Flush Portsee related information
Date Initiated by FirmSeptember 19, 2011
Date PostedMay 29, 2013
Recall Status1 Terminated 3 on May 30, 2013
Recall NumberZ-1428-2013
Recall Event ID 65083
510(K)NumberK050369 
Product Classification System,surgical,computer controlled instrument - Product Code NAY
ProductFlush Port (used in almost all da Vinci instruments) Assists in cleaning the instrument.
Code Information Model numbers: 340066-07 - straight; 340234-02 - extended taper; 340241-03 - 5mm; 340584-01 - Gemini 8mm straight; 340586-02 - Gemini 5mm; 340725-01 - Vespa straight; 340800-01 - Gemini ext taper; 340971-01 - IS1200 Grasping 340972-01 IS2000 Grasping.
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		Clarification of existing labeling information and operating procedures.
FDA Determined
Cause 2		Labeling False and Misleading
ActionIntuitive Surgical sent an "IMPORTANT PRODUCT NOTIFICATION" letter dated October 17, 2011 to all affected customers. The letter identified the product, problem, and actions to be taken by the customers. Contact Customer Service at 1-800-876-1310 for questions regarding this notice.
Quantity in CommerceNA
DistributionWorldwide Distribution- USA Nationwide and countries of: Argentina, Australia,Canada, Chile, China, Czech Republic, Egypt, India, Israel, Italy,Korea-Republic of, Poland, Qatar, Romania, Saudi Arabia, Singapore, Spain, Thailand, Turkey, and Venezuela.
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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