Intuitive Surgical, Inc. da Vinci X (IS4200) and Xi (IS4000) systems, which consists of finished devices Surgeon Console (SSC), Patient Cart (PSCART), Vision System (VSS) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
da Vinci X (IS4200) and Xi (IS4000) systems, which consists of finished devices Surgeon Console (SSC), Patient Cart (PSCART), Vision System (VSS)
Brand
Intuitive Surgical, Inc.
Lot Codes / Batch Numbers
Software version P10 (OS4 v10.0.0/A70_P10_B738) SOFTWARE, EMBEDDED RLS, IS4000 AND IS4200, A70_P10_B738 (Model: 610092-738) on Model Name/Model Number/UDI-DI: ASSY, PSCART, IS4000, 4-ARM, P10/380652-55/00886874110720, ASSY, SSC, IS4000, P10/380677-28/00886874110744, ASSY, VSS VISION SYSTEM, IS4000, P10/381121-45/00886874110898, ASSY, PSCART, IS4200, P10/380620-47/00886874115404, ASSY, VSC, IS4000, RECONDITIONED, P10/380721-15/00886874115343, ASSY, SSC, IS4000, RECONDITIONED, P10/380723-16/00886874115374
Products Sold
Software version P10 (OS4 v10.0.0/A70_P10_B738) SOFTWARE,EMBEDDED RLS,IS4000 AND IS4200,A70_P10_B738 (Model: 610092-738) on Model Name/Model Number/UDI-DI: ASSY,PSCART,IS4000,4-ARM,P10/380652-55/00886874110720, ASSY,SSC,IS4000,P10/380677-28/00886874110744, ASSY,VSS VISION SYSTEM,IS4000,P10/381121-45/00886874110898, ASSY,PSCART,IS4200,P10/380620-47/00886874115404, ASSY,VSC,IS4000,RECONDITIONED,P10/380721-15/00886874115343, ASSY,SSC,IS4000,RECONDITIONED,P10/380723-16/00886874115374
Intuitive Surgical, Inc. is recalling da Vinci X (IS4200) and Xi (IS4000) systems, which consists of finished devices Surgeon Console (SSC due to Inadvertent energy delivery from surgical system instrument if 1) Force bipolar and bipolar instruments installed on system 2) Force bipolar connected. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Inadvertent energy delivery from surgical system instrument if 1) Force bipolar and bipolar instruments installed on system 2) Force bipolar connected to Force Triad generator, bipolar not connected to generator 3) Yellow pedal associated with force bipolar is pressed, released with head in surgeon console 4) Blue pedal associated with bipolar is pressed, resulting in force bipolar energy delivery
Recommended Action
Per FDA guidance
On 09/20/22, correction notices were mailed to customers. Customers were advised of the following: 1) The system software version can be located on the Vision Cart Touchscreen in the Troubleshooting Tab. 2) Ensure all device users read and understand this notice. 3) Notice should be passed on to all those who need to be aware within your organization or to any organization where the potentially affected devices have been transferred. 4) Ensure proper instrument connections to the generator(s) and continue to follow all existing warnings and cautions found in user manuals 551400-15, USER MANUAL,SYS,P10,US,IS4000, 553873-07, USER MANUAL,I-A,MDR P10,IS4000-IS4200 and 554070-04, ADD,I-A,FORCE BIPOLAR,IS4000,IS4200. 5) Complete and return the acknowledgement form. 6) The recalling firm will follow-up with customers and schedule a software upgrade. 7) After the upgrade, inform all personnel that the software update/upgrade was completed. 8) If you have experienced this issue or require additional assistance, contact Technical Support: 800-876-1310, Option 1 (24/7) or customerservice@intusurg.com
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
AL, AK, AZ, CA, CO, FL, GA, IL, IN, IA, KY, LA, MD, MA, MI, MS, MO, NE, NV, NC, OH, PA, SC, TN, TX, WA, WI
Page updated: Jan 10, 2026