InjuryOBP
NEUROSTAR
Received May 20, 2025
Report 3004824012-2025-00016 · MDR key 22054232
Device
Generic name
Tms
Manufacturer
Neuronetics, Inc.Product problems
- Patient-Device Incompatibility
- Patient-Device Incompatibility
Patient
NA · Female
- Memory Loss/Impairment
- Memory Loss/Impairment
Narrative
Additional Manufacturer Narrative
SINCE THE REPORTER DID NOT RESPOND TO NEURONETICS' ATTEMPTED OUTREACH FOR ADDITIONAL INFORMATION, IT WAS IMPOSSIBLE TO CONDUCT A THOROUGH INVESTIGATION AND CONFIRM THAT THE PERSON WAS TREATED WITH A NEUROSTAR DEVICE. BASED ON THE INFORMATION PROVIDED NO CAUSE CAN BE ATTRIBUTED BUT REPORTING OUT OF AN ABUNDANCE OF CAUTION.
Description of Event or Problem
NEURONETICS' SOCIAL MEDIA MONITOR FORWARDED A POST ALLEGING TMS TREATMENT CAUSED THE REPORTER'S FRIEND TO HAVE MEMORY ISSUES.