MAUDE Adverse Event Report: Therabody, Inc. Therabody; Theragun G4 Pro charging stand

Model Number	G4
Medical Device Problem Code	Melted (1385)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	09/22/2025
Type of Reportable Event	Malfunction

• Brand Name: Therabody
• Common Device Name: Theragun G4 Pro charging stand
• Manufacturer (Section D): Therabody, Inc.; 1640 s.sepulveda blvd.; suite 300; los angeles 90025
• Manufacturer (Section G): Therabody, Inc.; 1640 s.sepulveda blvd.; suite 300; los angeles 90025
• Manufacturer Contact: cj frederick ; 1640 s.sepulveda blvd.; suite 300; los angeles 90025
• MDR Report Key: 50939330
• Report Number: 3012386142-2026-00008
• Device Sequence Number: 10759961
• Product Code: ISA
• UDI-Device Identifier: 00810036050135
• UDI-Public: 00810036050135
• Combination Product (Y/N): N
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Administrator/Supervisor
• Remedial Action: Recall
• Type of Report: Initial
• Report Date (Section B): 09/17/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Lay User/Patient
• Device Model Number: G4
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Received by Manufacturer: 09/22/2025
• Initial Report FDA Received Date: 09/29/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown