FDA Medical Device Recalls (openFDA)
Therabody, Inc: 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
- Recall number
- Z-2835-2026
- Recalling firm
- Therabody, Inc
- 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
- Status
- Open, Classified
- Initiated
- 2026-06-23
- Posted
- 2026-07-31
- Terminated
- not on file
- Reason
- 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.
- Root cause
- Under Investigation by firm
- Action
- On June 23, 2026, the firm sent a notice to all distributors, retailers, and resellers in the US and Canada titled "STOP SALE AND DISTRIBUTION NOTICE". Recipients were instructed to stop sale, distribution, and transfer of the charger for the Theragun G4 PRO in the United States and Canada. Product should be removed from shelves, displays, and online listings. Product should be segregated and inventory clearly marked as "DO NOT SELL - STOP SALE". Recipients are instructed to not return product to consumers or dispose of inventory. Firm is currently evaluating and addressing the issue.
- Quantity
- 584224
- Distribution
- Worldwide - US Nationwide distribution.
- Lot, serial or model codes
- UDI-DI 00810036050135 Charger GTIN 810036051378 All lots are recalled. Production ended in 2022.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- ISA
- Firm FEI
- 3012386142
- Firm city
- Los Angeles
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28