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Stop using now Medical device recall · FDA · Published June 23, 2026

Therabody Theragun G4 PRO Charger Fire Risk - Recall

Therabody recalls G4 PRO charger for fire risk due to overheating during charging. Affected units include specific models sold in 2022 and earlier. Stop using immediately to prevent fire.

🇺🇸 FDA recall #Z-2835-2026Medical deviceTherabody ›
✎ GovInfoNow plain-language explainer

Therabody is recalling chargers for their G4 PRO Theragun massage devices because the charger can overheat and cause fire. This risk is serious enough that users should stop using the charger immediately to avoid potential fire hazards. Read more at govinfonow.com/recall/314328-therabody-theragun-g4-pro-charger-fire-risk-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/314328-therabody-theragun-g4-pro-charger-fire-risk-recall · Updated August 18, 2026 · FDA enforcement record: FDA #Z-2835-2026

Cite this page

“Therabody Theragun G4 PRO Charger Fire Risk - Recall.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/314328-therabody-theragun-g4-pro-charger-fire-risk-recall. Based on FDA recall #Z-2835-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2835-2026%22&limit=1).

Therabody, Inc. recalled chargers for the Theragun G4 PRO and related products on June 23, 2026, after they may overheat and cause a fire, according to the FDA. Owners should stop using the chargers immediately.

How to tell if you have it

  • Therabody
  • Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO
  • upc 00810036051378

The hazard

The charging cradle for the device 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.

Context

GovInfoNow's records show Therabody has had prior recalls, including the 2026-03-23 Nerivio Infinity Software Version 4.1.2.0 Recall for charging risk of smoke and odor. Other recent recalls of similar products include the 2025-10-13 MRIMed MRI LED Mobile Exam Light Battery SL-111 for overheating risk during charging and the 2025-11-26 Medline Full Electric Low Bed Recall for rare fire risk from hand pendant overheating.

How to tell if you have this one

Check for the charger model with SKU numbers like TG02428-01, G4-PRO-PKG-NA, or PRO-CHARGER-SINGLE. The charger was sold in the US and Canada from 2022 or earlier.

  • Brand
    Therabody
  • Product
    Charger for the Therabody Theragun, G4 PRO massage device, and products which include the 4th Generation Theragun PRO
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Charger Now

    Immediately stop using the charger if it has been sold in the US or Canada from 2022 or earlier.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide - US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 50 days after the firm started it.

1. Firm started the recall: Jun 23, 202612. FDA classified it Class II: Jul 31, 202623. Published in FDA’s Enforcement Report: Aug 12, 202634. Added to GovInfoNow: Aug 18, 202642026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-2835-2026 (June 23, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2835-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA