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JOYSTICK

Aktormed GmbH · Model 141389 · UDI-DI 04260463843897

NAY Prescription
10
510(k) clearances
140,998
Adverse events (787 deaths)
248
Recalls
95
Facilities

Recalls

DateFirmReason
2026-04-24Intuitive Surgical, Inc.Due to unintentionally activated near infrared handheld camera when attempting to turn off illumination during normal clinical workflow transitions, particularly when switching fro
2026-04-22Intuitive Surgical, Inc.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 engage
2026-04-02Intuitive Surgical, Inc.Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.
2026-03-11Intuitive Surgical, Inc.Reloads for curved-tipped stapler may potentially produce an incomplete staple line.
2025-12-30Intuitive Surgical, Inc.Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth perception) but 2D maint
2025-12-15Intuitive Surgical, Inc.Access Port System tray may develop cracks potentially resulting in a sterility breach.
2025-12-09Intuitive Surgical, Inc.Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
2025-12-09Intuitive Surgical, Inc.Due to increased complaints for broken/frayed grip cables for reusable instruments.
2025-12-09Intuitive Surgical, Inc.Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
2025-12-09Intuitive Surgical, Inc.Due to increased complaints for broken/frayed grip cables for reusable instruments.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.