The Recall Desk

FDA (Devices) recall action 71718

Trumpf Medical Systems, Inc. recalled 5 products on 2015-08-19

The FDA (Devices) publishes a recall like this one as 5 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 5 pages.

Products
5
Announced
2015-08-19
Critical
0
Units
46,435

Why these products were recalled

Complaints received of the front joint of the spring arm AC 2000 could break at the interface to the monitor.

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

States named across these recalls

1–5 of 5

  • HighFDA (Devices)··2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled for Joint Breakage Risk

    Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,TruVidia HD, User Manual #1513140. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Distribution
    1 state
  • HighFDA (Devices)··2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled for Spring Arm Defect

    Trumpf Medical Systems is recalling TruLight 3000/5000 surgical lights because the front joint of the spring arm could break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,TruLight 3000/5000, User Manual #1528403. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Distribution
    1 state
  • HighFDA (Devices)··2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled Due to Spring Arm Defect

    Trumpf Medical Systems is recalling 9,287 ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,Helion/Xenion S/M/L, User Manual #1441784. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Distribution
    1 state
  • HighFDA (Devices)··2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled Due to Joint Breakage Risk

    Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,TruVidia SD, User Manual #1400191. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Distribution
    1 state
  • HighFDA (Devices)··2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled for Spring Arm Defect

    Trumpf Medical Systems is recalling 9,287 surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,iLED 3/5, User Manual #1558932. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Distribution
    1 state