The Recall Desk

Manufacturer

Trumpf Medical Systems, Inc.

30 recalls in our database name Trumpf Medical Systems, Inc. as the manufacturing or recalling firm.

What the numbers show

Total
30
Critical
0
Severe
4
Most recent
2018-03-07

Of the 30 recalls from Trumpf Medical Systems, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 4 (13%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

26–30 of 30

  • HighFDA (Devices)·Z-0141-2015·2014-11-05

    Trumpf TITAN Operating Room Table Recalled for Unintended Movement

    Trumpf Medical Systems is recalling 184 TITAN Operating Room Tables due to unintended movement during surgery caused by damaged remotes.

    Product
    TITAN Operating Room Table Patient positioning during surgery, ranging from anesthesia induction to actual surgery to recovery from anesthesia. Patient transport on the operating tabletop, from the patient transfer system to the operating theatre or from the operating theatre
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0484-2014·2013-12-18

    Trumpf Medical Systems Recalls Helion S and H300 Exam Lights

    Trumpf Medical Systems is recalling 287 Helion S and H300 exam lights because a plastic joint may fail due to fatigue after seven years of use.

    Product
    Helion S Exam Light or H300 The device is intended to locally illuminate an examination area of the patient's body with high intensity light in a clinic or doctor's practice.
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0342-2014·2013-11-27

    Trumpf TruSystem Surgical Table Leg Section Recall for Detachment Risk

    Trumpf Medical Systems is recalling 15 TruSystem Surgical Table Leg Section One Part Light components because the coupler point may detach from the frame.

    Product
    TruSystem Surgical Table (TS7000)  Leg Section One Part Light HU Use of the Leg Section One Part Light HU is permitted only with the TRUMPF TruSystem 7000 operating table. The operating table TruSystem 7000, in conjunction with operating table components is intended for the u
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0077-2013·2012-10-24

    Trumpf Medical Systems Recalls Helion and Xenion Surgical Lights

    Trumpf Medical Systems is recalling 275 Helion and Xenion surgical lights due to reported fractures of the front joint of the spring arm.

    Product
    Helion and Xenion surgical lights, 501/01 series KLM lights. The surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2311-2012·2012-09-12

    Trumpf Acrobat 3000 Spring Arm Recalled for Welded Seam Cracks

    Trumpf Medical Systems is recalling Acrobat 3000 spring arms for iLED operating lights because cracks can form on the welded seam at the rear joint.

    Product
    Acrobat 3000 (AC3000) Spring Arm as support arm for iLED operating lights, TRUMPF Medizinsysteme GmbH + Co KG 82178 Puchheim. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.
    Category
    Medical Device
    Distribution
    7 states