da Vinci SP Endoscope, 0° 430600Recalls & reported problems
Intuitive Surgical, Inc. · Endoscope, 0° · Class 2
All models of da Vinci Surgical System (9)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00886874123188), received between Jan 14, 2026 and Jan 14, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Display or Visual Feedback Problem” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Display or Visual Feedback Problem1
Patient problems
- Unspecified Tissue Injury1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 14, 2026Display or Visual Feedback Problem
IT WAS REPORTED THAT DURING A DA VINCI-ASSISTED SURGICAL PROCEDURE, THE IMAGE THROUGH THE ENDOSCOPE WENT BLACK. THE CUSTOMER DID NOT HAVE A BACKUP ENDOSCOPE AVAILABLE FOR TROUBLESHOOTING. THE CUSTOMER REPORTEDLY HAD AN INSTRUMENT ON THE PATIENT'S GALL BLADDER. THE INTUITIVE SURGICAL, INC. (ISI) TECHNICAL SUPPORT ENGINEER (TSE) ASKED IF THEY COULD VISUALIZE THE INSTRUMENTS AND IF THEY HAD A THIRD PARTY SCOPE TO USE. THE SURGICAL STAFF PROCEEDED WITH LAPAROSCOPIC SCOPE AND THE TSE WALKED THE CUSTOMER THROUGH REMOVING INSTRUMENTS MANUALLY. THE CUSTOMER WAS ABLE TO REMOVE THE INSTRUMENTS AND UNDOCK FROM THE PATIENT. THE CUSTOMER TRIED POWER CYCLING THE SYSTEM BUT THE ENDOSCOPE WOULD NOT PASS A SELF-TEST. THE CUSTOMER THEN ELECTED TO CONVERT THE PROCEDURE TO MULTI-PORT SURGERY IN ORDER TO COMPLETE THE CASE.
Patient problems: Unspecified Tissue Injury
MAUDE report 24072341 ↗
Other System, surgical, computer controlled instrument devices
- EndoWrist 471205Intuitive Surgical, Inc. · System, surgical, computer controlled instrument1 recall14,225 reports
- EndoWrist 470179Intuitive Surgical, Inc. · System,surgical,computer controlled instrument2 recalls2 deaths10,156 reports
- EndoWrist 471093Intuitive Surgical, Inc. · System, surgical, computer controlled instrument1 recall8,581 reports
- EndoWrist 471172Intuitive Surgical, Inc. · System, surgical, computer controlled instrument1 recall1 death6,302 reports
- daVinci Xi 380652Intuitive Surgical, Inc. · System,surgical,computer controlled instrument2 recalls235 deaths5,316 reports
- daVinci Xi 381121Intuitive Surgical, Inc. · System,surgical,computer controlled instrument1 recall2 deaths4,310 reports
- EndoWrist 471405Intuitive Surgical, Inc. · System, surgical, computer controlled instrument1 recall1 death3,770 reports
- EndoWrist 470327Intuitive Surgical, Inc. · System,surgical,computer controlled instrument2 recalls2,273 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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