The Recall Desk

Hazard

Laser Radiation recalls

10 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
10
Critical
0
Severe
1
Most recent
2023-07-05

Of the 10 laser radiation recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (10%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all laser radiation recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

1–10 of 10

  • HighFDA (Devices)·Z-1971-2023·2023-07-05

    Integre Pro Laser Ophthalmoscope Systems: Risk of Unintended Laser Emission

    Ellex Medical is recalling certain Integre Pro laser ophthalmoscope systems because scattered laser radiation may unintentionally exit the device and be emitted from the objective lens, potentially exposing users' eyes to unexpected laser energy.

    Product
    Integre Pro Yellow LP561, Integre Pro Yellow LP6RY, Integre Pro Scan Green LP6G, Integre Pro Green LP5532 Spare, Optics Bench V2, L2G/LP6G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0001-2022·2021-11-03

    RAPTAR Laser Range Finders Recalled for Field Modification Safety Risk

    Potomac River Group recalls 62 RAPTAR Laser Range Finders (Model G02) nationwide. The devices can be field-modified to enable higher-power visible and infrared lasers, posing eye injury risk from uncontrolled laser radiation.

    Product
    RAPTAR Laser Range Finders
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2497-2020·2020-07-15

    Ra Medical Systems Recalls DABRA Laser Due to Software Issue

    Ra Medical Systems is recalling 79 DABRA Laser units because a software issue could cause unintended laser light release, potentially injuring users or patients.

    Product
    DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Catheter is an excimer laser ultraviolet light source and delivery system, collectively the DABRA Laser System". The system is designed to deliver the energy to the surgical site to ablate unwanted material. The optica
    Category
    Medical Device
    Distribution
    22 states
  • HighFDA (Devices)·Z-0681-2020·2020-01-08

    DeWALT and Stanley Laser Distance Measurers Recalled for Excessive Radiation

    Stanley Black & Decker is recalling specific DeWALT and Stanley laser distance measurers because they may emit laser radiation exceeding Class II safety limits.

    Product
    The products involved are DeWALT laser distance measurers, model numbers DW0165, DW0165S, DW0330S and Stanley Fatmax FMHT77506. These products were produced for DeWALT and Stanley by a contract manufacturer.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2093-2019·2019-08-14

    Gk Photonics Atom Laser Projection Series Recalled for Safety Compliance

    Gk Photonics Inc is recalling the Atom Laser Projection Series because the provided remote interlock dongle does not fully comply with FDA manual reset requirements, posing a risk of high-power laser exposure.

    Product
    Atom Laser Projection Series
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2095-2019·2019-08-14

    Gk Photonics Maxim Laser Projection Series Recalled for Safety Defect

    Gk Photonics is recalling the Maxim Laser Projection Series because the provided remote interlock dongle may not fully comply with FDA safety requirements, potentially exposing users to high-power laser radiation.

    Product
    Maxim Laser Projection Series
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2096-2019·2019-08-14

    Gk Photonics Logolas Laser Projectors Recalled for Safety Interlock Defect

    Gk Photonics is recalling Logolas Laser Projection Series units because the remote interlock dongle may not fully comply with FDA safety requirements, posing a risk of high-power laser exposure.

    Product
    Logolas Laser Projection Series
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2097-2019·2019-08-14

    Gk Photonics Recalls Burstberry Laser Projection Series for Safety Defect

    Gk Photonics Inc is recalling the Burstberry Laser Projection Series because the provided remote interlock dongle fails to meet FDA safety requirements, posing a risk of high-power laser radiation exposure.

    Product
    Burstberry Laser Projection Series
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2094-2019·2019-08-14

    Gk Photonics Spectrum Laser Projection Series Recalled for Safety Defect

    Gk Photonics is recalling the Spectrum Laser Projection Series because the included remote interlock dongle may fail to prevent high-power laser radiation exposure.

    Product
    Spectrum Laser Projection Series
    Category
    Medical Device
    Distribution
    0 states