FDAFDA recall Z-2835-2026 · Aug 12, 2026
Therabody, Inc: Charger for the Therabody Theragun recall
Recall found
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
Reason for recall
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 to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- UDI-DI 00810036050135 Charger GTIN 810036051378 All lots are recalled. Production ended in 2022.
- Quantity
- 584224
- Distribution
- Worldwide - US Nationwide distribution.
- Recalling firm
- Therabody, Inc, Los Angeles, CA
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-06-23
Source: openFDA enforcement record Z-2835-2026 · search recall number Z-2835-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.