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U.S. Department of Health and Human Services

Class 2 Device Recall Firefly

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  Class 2 Device Recall Firefly see related information
Date Initiated by Firm November 21, 2014
Date Posted December 19, 2014
Recall Status1 Terminated 3 on February 20, 2015
Recall Number Z-0835-2015
Recall Event ID 69845
510(K)Number K141077  
Product Classification Laparoscope, general & plastic surgery - Product Code GCJ
Product Fluorescence Imaging Procedure Kit, designed
for use with Firefly Fluorescence Imaging for the da Vinci Xi 4000 Surgical Systems. The Intuitive Surgical Endoscopic Instrument Control System (Intuitive Surgical da Vinci Surgical System Model IS3000) is intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
Code Information PN 950156-02
Recalling Firm/
Manufacturer
Intuitive Surgical, Inc.
1266 Kifer Rd Bldg 100
Sunnyvale CA 94086-5304
For Additional Information Contact Mark Johnson
408-523-2100
Manufacturer Reason
for Recall
The storage conditions for indocyanine green (ICG) are not on the individual Fluorescence Imaging Procedure Kit box, the six-kit box, and the shipping box. If heat were to damage the material, the result would be a loss of fluorescence.
FDA Determined
Cause 2
Labeling design
Action Urgent Medical Device Correction Letters were sent to customers on November 24, 2014.
Quantity in Commerce 1532
Distribution Nationwide Distribution.
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 = GCJ and Original Applicant = INTUITIVE SURGICAL, INC.
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