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LightForce FXi LTC-1500Recalls & reported problems

Litecure LLC · Infrared phototherapy device emitting up to 15 W at 980/810nm in CW or pulsed modes. The device can be powered through its battery pack or mains power and has a 10" touch-screen display. · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00854103007042), received between Mar 20, 2019 and Mar 20, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Improper or Incorrect Procedure or Method1

Patient problems

  • Radiation Burn1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 20, 2019Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

    PATIENT DEVELOPED BLISTER ON FOOT THAT MAY HAVE BEEN CONTRIBUTED TO BY THE SUBJECT DEVICE.

    Patient problems: Radiation Burn

    MAUDE report 8437489 ↗

Other Lamp, Infrared, Therapeutic Heating devices

All Lamp, Infrared, Therapeutic Heating devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.