The Recall Desk

Manufacturer

Lumenis Limited

3 recalls in our database name Lumenis Limited as the manufacturing or recalling firm.

What the numbers show

Total
3
Critical
0
Severe
0
Most recent
2016-11-02

Of the 3 recalls from Lumenis Limited we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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.

1–3 of 3

  • HighFDA (Devices)·Z-0301-2017·2016-11-02

    Lumenis Recalls FemTouch Delivery System Due to Ineffective Cleaning Instructions

    Lumenis Limited is recalling 69 units of the FemTouch delivery system because the provided cleaning instructions may be ineffective for fully assembled devices, posing a risk of cross-contamination.

    Product
    FemTouch delivery system includes the FemTouch Kit (AC-1007415) and FemTouch" Tip (SPSA-20002590) Provide fractional treatments in gynecology.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1519-2015·2015-05-06

    Lumenis Light Sheer Desire Diode Laser System Recalled for Software Error

    Lumenis is recalling 117 Light Sheer Desire Diode Laser Systems because software parameters exceed manual settings, potentially causing burns.

    Product
    Light Sheer Desire Diode Laser System with XC Handpiece Accessory options.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0795-2013·2013-02-20

    Lumenis Recalls VersaCut Tissue Morcellator for Labeling Corrections

    Lumenis Limited is recalling VersaCut Tissue Morcellator devices to correct labeling following three reported air embolism events caused by incorrect tubing hook-up.

    Product
    The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for use under direct or endoscopic visualization for the morcellation and removal of dissected tissue during pelviscopic, laparoscopic, percutaneous, and open surgical procedures whenever access to the surgi
    Category
    Medical Device
    Distribution
    Distributed nationwide

About this company

Community-sourced company facts from Wikidata, not from any recall agency. This is background on the corporate entity — it says nothing about the recall(s) listed on this page, which come from the agency source notice above.

Lumenis

company that develops and manufactures minimally-invasive clinical solutions for the Surgical, Ophthalmology & Aesthetic markets

Country
Israel
Founded
1991

Official website

Source: Wikidata (Q4043248), licensed CC0. Wikidata is community-edited and may not reflect the current corporate structure.