FDA Recall Terminated

da Vinci Si Surgical System, IS3000; - Wall chart for EndoWrist Stapler 45 System. Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Recall: Z-1048-2015 · Initiated January 15, 2015

Recall

Recall Number
Z-1048-2015
Event Number
70181
Firm
Intuitive Surgical, Inc.
FEI Number
3001675293
Product Code
NAY
Status
Terminated
Root Cause
Error in labeling
Initiated
January 15, 2015
Posted
February 3, 2015
Terminated
March 3, 2015
Address
1266 Kifer Rd, Bldg 100, Sunnyvale, CA, 94086-5304

Description

da Vinci Si Surgical System, IS3000; - Wall chart for EndoWrist Stapler 45 System. Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.

Reason

The Wall chart has been updated because it was noted that Wall Chart (PN 551524-03 Rev A) was inconsistent with the User Manual Adendum (PN 550986-07_B) with regards to neceassary sterilization dry time.

Action

Medical Device Recall Replacement letters were sent to all customers on January 15, 2015. The letter identified the reason for the recall, the risk to health, affected products, and actions to be taken by the customer or user and the firm. Customers were asked to discard the existing EndoWrist Stapler Documentation and replace it with the new Documentation provided by the firm. Intuitive Surgical will ship replacement instruments at no charge to customers. Then customers were asked to reunite the replacement instruments with the additional components. The firm will retrain customers on the updated instructions for use. A Clinical Sales Representative or Intuitive Surgical Customer Service at 1-800-876-1310, should be contacted if further information or support is needed concerning the recall notification.

Distribution

Nationwide Distribution

Quantity

1,034