Force Feedback 475049Recalls & reported problems
Intuitive Surgical, Inc. · Force Feedback Cadiere Forceps · Class 2
All models of Force Feedback (11)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00886874120712), received between Dec 27, 2024 and Jul 7, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Material Frayed1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 7, 2025Material Frayed; Material Frayed
REFER TO H11 FOR FOLLOW-UP INFORMATION.
Patient problems: Insufficient Information
MAUDE report 22421183 ↗MalfunctionDec 27, 2024Break; Break
IT WAS REPORTED THAT DURING CENTRAL PROCESSING, THE SHAFT WAS BROKEN OFF FROM THE FORCE FEEDBACK CADIERE FORCEPS. THERE WAS NO REPORTED PATIENT IMPACT OR HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21024345 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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