FDA Medical devices recall ·
Charger for the Therabody Theragun, G4 PRO massage device… recall
- Recall number
- Z-2835-2026
- Date
- (initiated June 23, 2026)
- Company / brand
- Therabody, Inc
1640 S Sepulveda Blvd Ste 300, Los Angeles, CA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 584224
- Hazard tags
- Fire Burn
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO charger. G4 PRO Black US - Refurb., SKU TG02428-01 G4 PRO NA, SKU G4-PRO-PKG-NA G4-PRO-PKG-US, SKU G4 PRO US G4 PRO Black US - Refurb V, SKU TG0002428-1V10 Pro Charger Single Unit, SKU PRO-CHARGER-SINGLE
Why was it recalled?
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 overheating.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI-DI 00810036050135 Charger GTIN 810036051378 All lots are recalled. Production ended in 2022.
Distribution
Worldwide - US Nationwide distribution.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-2835-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.