Intuitive Surgical, Inc. da Vinci S Surgical System, Model number IS2000 Revision number A51 P5; endoscopic surgical control system, Intuitive Surgical, Inc., Sunnyvale, CA 94086 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
da Vinci S Surgical System, Model number IS2000 Revision number A51 P5; endoscopic surgical control system, Intuitive Surgical, Inc., Sunnyvale, CA 94086
Brand
Intuitive Surgical, Inc.
Lot Codes / Batch Numbers
Model number IS2000, Revision AP51 P5, System numbers SG015, SG020, SG040, SG103, SG152, SG169, SG179, SG213, SG215, SG355, top level part numbers 380267-01, 380431-02, and 380431-05
Products Sold
Model number IS2000, Revision AP51 P5, System numbers SG015, SG020, SG040, SG103, SG152, SG169, SG179, SG213, SG215, SG355, top level part numbers 380267-01, 380431-02, and 380431-05
Intuitive Surgical, Inc. is recalling da Vinci S Surgical System, Model number IS2000 Revision number A51 P5; endoscopic surgical control due to Delay in responding: In certain circumstances, the device may not respond immediately to a user's command such as master clutch or camera control.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Delay in responding: In certain circumstances, the device may not respond immediately to a user's command such as master clutch or camera control.
Recommended Action
Per FDA guidance
Beginning 12/28/2007, Intuitive Surgical Field Service Representatives visited each site to correct the issues. A notification letter was provided to all sites.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, HI, MI, NV, NH, NJ, TX, WA
Page updated: Jan 10, 2026