Therabody Theragun Charger Recall Issued
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Therabody, Inc. is recalling 584,224 chargers for the Theragun G4 PRO due to a risk of overheating and fire.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 19, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Devices.
What Happened
The charging cradle for the Theragun G4 PRO may overheat while charging the device's removable battery pack, presenting a risk of thermal event (fire). The firm has received reports alleging the product caught fire and other reports regarding visible smoke, melting, charger burn, burning odor, and overheating.
Which Products Are Affected
The recall involves the Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO charger. Affected SKUs include: 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. A total of 584,224 units are affected. All lots are recalled. Production ended in 2022. UDI-DI 00810036050135, GTIN 810036051378. Distribution is US Nationwide and worldwide.
What You Should Do
Consumers should follow guidance from the recalling firm regarding the affected chargers.
Why This Matters
The recall addresses a potential fire hazard associated with the charger for the Theragun G4 PRO device.
Source
FDA recall number Z-2835-2026. Classification: Class II. Recalling firm: Therabody, Inc., Los Angeles, CA.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,266 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 19, 2026.
Frequently Asked Questions
Common questions about this FDA recall.