Fresh Recalls

FDAClass II · Medical device · Recall Z-2835-2026 · Recalled August 12, 2026

Charger for the Therabody Theragun recall — Therabody, Inc

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Charger for the Therabody Theragun
Company / brand
Therabody
Lot / serial / date codes
UDI-DI 00810036050135 Charger GTIN 810036051378 All lots are recalled. Production ended in 2022.
Distribution
Worldwide - US Nationwide distribution.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: 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.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Charger for the Therabody Theragun

3. Open the official notice or contact

Official recall ID
Z-2835-2026
Brand
Therabody
Classification
Class II
Units affected
584,224
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Los Angeles, CA, United States
Firm address
1640 S Sepulveda Blvd Ste 300, 90025-7565

Identifying details (verbatim from the notice)

Product codes / lots
UDI-DI 00810036050135 Charger GTIN 810036051378 All lots are recalled. Production ended in 2022.
Distribution
Worldwide - US Nationwide distribution.
Firm notified the public via
E-Mail
FDA event ID
99281
Recall initiated
June 23, 2026
FDA classified
July 31, 2026
FDA report date
August 12, 2026
Verify with the official sources:

Found something wrong or missing? Report a data error.

Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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