Z-2835-2026Class II

Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation...

Name: Z-2835-2026 Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation...
Creator: Therabody, Inc
Published: 2026-06-23
License: https://open.fda.gov/license/

Therabody, Inc. / initiated 2026-06-23 / Open, Classified

FDA source

Therabody, Inc began a recall of 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... on 2026-06-23. FDA classified it as Class II and gives the reason as "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...". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-2835-2026
Classification: Class II
Status: Open, Classified
Initiated: 2026-06-23
Posted: 2026-07-31
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
Product code: ISA Massager, Therapeutic, Electric
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.
FDA 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 in commerce: 584224
Distribution: Worldwide - US Nationwide distribution.
Product codes and lots: UDI-DI 00810036050135 Charger GTIN 810036051378 All lots are recalled. Production ended in 2022.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-2835-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-2835-2026	Class II	Ongoing	Voluntary: Firm initiated	2026-08-12	2026-07-31

Product code ISA

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)