Overview of recall records associated with Intuitive Surgical, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 103, Class I: 1.
Robotic-assisted surgical system arm drapes may detach from the instrument arm due to an issue involving the drape rings located at the top of the product, which may expose a section of…
Operative components of surgical systems potentially distributed with E-brake retainer pin, so in event of a structural column failure, the E-brake pin would prevent E-brake engagement and…
Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching from the…
Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.
Reloads for curved-tipped stapler may potentially produce an incomplete staple line.
Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Due to increased complaints for broken/frayed grip cables for reusable instruments.
Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
An error event following the release of a software version for the surgical system that can result in loss of user interface content on an external monitor or tower monitor.
Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth perception) but 2D maintained, or…
Due to a software implementation error that allowed instruments arms failing an important diagnostic test to remain in clinical use. This test was supposed to be used to detect Universal…
Due to probe bags that may have a compromised or incomplete sterile pouch seal.
Access Port System tray may develop cracks potentially resulting in a sterility breach.
Surgical system Error 23062 due to connector1) Partially damaged "Potential problem with ergonomics: Disable - Retry " or 2) Failed "Disable Ergonomics: Viewer, headrest, armrest, and pedal…
Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
This page summarizes recall records in which the official source identifies Intuitive Surgical, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
