RecallRadar

FDA Device recall Z-2835-2026

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

On 2026-08-12 the FDA classified a Class II recall of Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO charger by Therabody, citing 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 pro….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2835-2026
ClassificationClass II
Statusongoing
Initiated2026-06-23
Published2026-08-12
Last updated2026-09-13 11:58 UTC
CompanyTherabody
DistributionUS

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

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.

Identifiers

code_infoUDI-DI 00810036050135 Charger GTIN 810036051378 All lots are recalled. Production ended in 2022.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2835-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.