RegWardenFDA facility compliance records
Facility

Therabody, Inc.

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2026: 1 recalls20172018201920202021202220232024202512026
  • Recalls (1)

Devices registered here (3)

  • Light Based Over The Counter Wrinkle Reduction
    Product code OHS (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4810
  • Vibrator, Therapeutic
    Product code IRO (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.5975
  • Over-The-Counter Powered Light Based Laser For Acne
    Product code OLP (opens in a new tab) · Class II · General, Plastic Surgery · 21 CFR 878.4810

Recalls & enforcement

  • Class IIOngoing2026-06-23
    Charging cradle for the device may overheat while charging the device's removable battery pack, presenting risk of thermal event (fire). Firm has received reports alleging the product caught fire and other reports regarding visible smoke, melting, charger burn, burning odor, and …

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Therabody, Inc. (FEI 3012386142) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3012386142-therabody-inc/

Not open yet

Alerts for Therabody, Inc.

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.