Case type Defective Medical Devices

Surgical Robot Injuries

Surgeons operating in a modern operating room with monitors overhead.

Injured during robot-assisted surgery? Tell us your story.

CBW Law reviews claims from people injured during robot-assisted surgery when a system or instrument may have failed. Tell Us Your Story. Contacting us does not create an attorney-client relationship.

Tell Us Your Story Call (800) 476-2416

In robot-assisted surgery, a surgeon controls instruments on mechanical arms from a console. Injuries during these operations can come from the platform, from an instrument such as a stapler or energy tool, from surgical technique or from the patient's condition. Recalls often involve the instruments. A surgical robot lawyer works to find out which one caused the harm.

What robot-assisted surgery is

In robot-assisted surgery, the surgeon sits at a console and uses controls to move instruments attached to mechanical arms, usually through small incisions. The FDA notes the device is not actually a robot because it can't perform surgery without direct human control1. A system usually includes1:

  • A console, where the surgeon views a 3-D image and controls the instruments
  • One or more bedside carts with arms, a camera and instruments
  • A separate cart with supporting equipment, such as an electrosurgical unit that powers cutting and sealing tools

The FDA has cleared these systems for laparoscopic procedures in general, heart, colorectal, gynecologic, head and neck, chest and urologic surgery. Common examples include gallbladder removal, hysterectomy and prostate removal1.

Platform, instruments or technique

An injury during robot-assisted surgery doesn't mean the robot malfunctioned. A review separates several possible sources:

Where a problem can start
SourceExamplesTypical evidence
The platform System faults, interruptions, camera problems System event logs and service records
Instruments and accessories Broken instruments, insulation failures in energy tools, stapler problems Instrument names and lot numbers, operative report
Surgical technique Choices and actions by the surgical team Operative report, video if recorded
The patient's condition Anatomy, disease and healing Medical history and imaging

Claims about the platform or instruments are product claims. Claims about technique or training follow medical malpractice rules. Some cases involve both.

The FDA says robot-assisted surgery is safe and effective for certain procedures when used appropriately and with proper training, and that patients may ask about their surgeon's training and experience with these devices1. It also says no robot-assisted surgical system has been authorized specifically to prevent or treat cancer1.

Instrument problems and recalls

Recalls often involve instruments rather than the main system. In 2026, Intuitive Surgical recalled 8 mm SureForm 30 Gray reloads for its curved-tip stapler. It reported incomplete staple lines on blood vessels even though the da Vinci system showed a completed stapler fire. Incomplete staple lines on a vessel can cause bleeding that may require converting to open surgery. As of Feb. 23, 2026, Intuitive had reported four serious injuries and one death, and it told hospitals to stop using and quarantine the affected reloads2.

Staplers have their own page: surgical stapler and clip injuries.

Robot-assisted surgery at a glance

Who controls it
The surgeon, at all times1.
Common procedures
Gallbladder removal, hysterectomy, prostatectomy.
Recall example
SureForm 30 Gray stapler reloads, 20262.
Key question
Platform, instrument or technique?

Injuries that lead to review

  • Burns or holes in the bowel, bladder, blood vessels or other organs
  • Bleeding that required more surgery or transfusion
  • A procedure converted to open surgery because of an equipment problem
  • A broken instrument piece left in the body
  • Infection, sepsis or a long hospital stay after a device problem

A complication can happen in any surgery, robotic or not. What matters is whether the records point to a device problem, such as a documented alarm, a broken instrument or an instrument from a recalled lot.

Who may have a surgical robot claim

  • The operative report notes an equipment malfunction or alarm
  • An instrument from a recalled lot was used
  • A repair surgery found an injury consistent with an instrument failure
  • The team had to stop or convert the procedure because of the equipment

Who may be responsible

An investigation may look at the maker of the system or instrument involved. The hospital and surgical team are reviewed separately under medical malpractice rules, which have their own notice and filing requirements in many states.

Filing deadlines for surgical robot lawsuits

Deadlines depend on your state and on when you learned of the injury and its possible cause. Examples:

  • Arizona: generally two years for personal injury and wrongful death3.
  • California: two years for injury to or death of a person caused by another's wrongful act or neglect4.
  • New York: three years for personal injury5, with a separate rule that runs from discovery for injuries caused by the latent effects of exposure to a substance in the body6.
  • Texas: two years for personal injury and wrongful death7, and most product liability claims must be brought within 15 years of the product's sale8.

Claims against hospitals and surgeons often have their own shorter deadlines and notice rules. Ask a surgical robot attorney to check your dates early, because system logs and instruments may not be kept forever.

Tell Us Your Story →

Records that help a surgical robot review

Records worth gathering

Surgery

  • Operative report
  • Name of the robotic system
  • Instrument list, if available

Problems

  • Notes of any alarm, malfunction or conversion
  • Post-operative imaging
  • Repair surgery reports

Requests

  • Ask the hospital in writing to keep any surgical video and device logs

What happens after you contact CBW Law

How a review works

  1. Tell us what happened

    Share what you remember about the surgery, the problem and the treatment that followed. You do not need every record first.

  2. We identify the device

    We work to confirm the maker, model and lot or serial number, and whether any recall or safety notice covers it.

  3. We gather records

    With your permission, we request operative reports, imaging, device data and other records from your providers.

  4. We explain what we see

    We tell you what the records show, what questions remain and what options may be open, including deadlines.

A complication during robot-assisted surgery is not, by itself, proof that the robot or an instrument failed.

Plain English

Medical, Health & Insurance

Terms you may see in a surgical robot case.

Equipment

Console
Where the surgeon sits to control the instruments1.
Electrosurgical unit
Equipment that powers tools that cut or seal tissue with electric current.
Reload
A replaceable cartridge of staples for a surgical stapler.

Injuries

Thermal injury
A burn to tissue from an energy instrument.
Perforation
A hole in an organ or vessel.

Procedures

Conversion to open
Switching from small incisions to a larger open incision during surgery.

Questions

Surgical robot lawsuit questions

Short answers to the questions people ask first.

Does a robot perform the surgery?

No. The FDA says the surgeon controls the device at all times.

Was the robot involved in my injury, or just used during surgery?

That's the key question. A surgical robot lawyer looks for evidence of a device problem in the records.

Which instrument was involved?

The operative report and hospital records may list instruments and lot numbers.

Did the team document a malfunction?

Operative notes often record alarms, faults or a switch to open surgery.

Can I get the surgery video?

Some surgeries are recorded. Ask the hospital in writing to keep any video and logs.

Is a surgical robot claim a malpractice claim?

It can be a product claim, a malpractice claim or both, depending on what caused the injury.

Do I need a surgical robot attorney if I needed repair surgery?

A repair surgery report is important evidence. A surgical robot attorney can review it.

How long do I have to file a surgical robot lawsuit?

It depends on your state and the type of claim. Malpractice claims often have shorter deadlines.

Is robotic surgery approved to treat cancer?

The FDA says no robot-assisted system has been authorized specifically to prevent or treat cancer, though it is used in some cancer operations.

What does it cost to contact CBW Law?

Telling us your story costs nothing, and contacting us does not create an attorney-client relationship.

Tell Us Your Story

If you were injured during robot-assisted surgery, a surgical robot attorney can review what happened.

Tell us what happened. CBW Law will review your information and explain what we see. Submitting information does not establish an attorney-client relationship or guarantee representation.

Tell Us Your Story Call (800) 476-2416

This page is general information about robot-assisted surgery injuries. It is not legal or medical advice and does not create an attorney-client relationship. A complication during robot-assisted surgery does not, by itself, establish that a device malfunctioned or that anyone is legally responsible. Laws and deadlines differ by state, and no outcome can be promised.

Keep reading

Official resources

Government sources for device recalls, safety notices and reporting.

Government

Medical Device Recalls and Early Alerts, FDA

The FDA's list of serious device recalls.

Government

Report a device problem (MedWatch), FDA

Tell the FDA about a problem with a device.

Government

Computer-Assisted Surgical Systems, FDA

How robot-assisted surgery works.

Apparatus

Sources & Cited Articles

The source material behind each factual, medical and legal statement on this page, numbered to match the markers in the text.

  1. Computer-Assisted Surgical SystemsU.S. Food and Drug Administration · FDA.gov, content current as of Nov. 2, 2026; verified Nov 12, 2026Robotically-assisted surgical devices are controlled by the surgeon and can't operate without direct human control; components; cleared uses; no RAS device authorized specifically to prevent or treat cancer; patients may ask about training and experience.
  2. Surgical Stapler Reload Recall: Intuitive Surgical Removes 8mm SureForm 30 Gray ReloadsU.S. Food and Drug Administration · FDA recall notice, content current as of May 5, 2026; verified Nov 12, 2026Incomplete staple lines on blood vessels after the da Vinci system reports a completed fire; bleeding that may require conversion to open surgery; four serious injuries and one death reported as of Feb. 23, 2026.
  3. A.R.S. § 12-542Arizona State Legislature · Arizona Revised Statutes; verified Nov 12, 2026Two years for injury to the person and for wrongful death.
  4. Code of Civil Procedure § 335.1California Legislature · California Code; verified Nov 12, 2026Two years for injury to or death of an individual caused by the wrongful act or neglect of another.
  5. Civil Practice Law and Rules § 214New York State Senate · Consolidated Laws of New York; verified Nov 12, 2026Three years for personal injury.
  6. Civil Practice Law and Rules § 214-cNew York State Senate · Consolidated Laws of New York; verified Nov 12, 2026Latent effects of exposure to a substance: three years computed from discovery of the injury.
  7. Civil Practice and Remedies Code § 16.003Texas Legislature · Texas Statutes; verified Nov 12, 2026Two years for personal injury and wrongful death.
  8. Civil Practice and Remedies Code § 16.012Texas Legislature · Texas Statutes; verified Nov 12, 2026Products liability actions within 15 years of sale, with an exception for certain latent diseases from exposure.

Accountability

Reviewed by

Craig Weiss, founder and managing attorney of CBW Law Firm

Craig Weiss

Managing Attorney · CBW Law

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