FDA recall Z-1942-2024

WAVi Co. · Class II · device

Product

WAVi Research EEG Desktop System is comprised of the WAVi Research EEG Desktop Software with Instruction Manual and Brochure, and Heart Rate Variability (HRV) Ear Clips. The system kit also incorporates use of the firm's cleared EEG analysis technology (the WAVi SCAN EEG System and Accessories, and the WAVi Headset and eSoc Single Use Electrode Contacts).

Reason for recall

Following an FDA-issued Warning Letter, the firm requested return of their research EEG system components due to the closing of their research study.

Distribution

US: NC, TX, IL, NV, AZ, NY, CA, MI, KS, AL, FL, MD, UT, WA, PA, GA, AR, NM, CO, IA, CT, IN, VA, LA, HI, MA, OH, OR, MO, KY, ID

Key facts

Status
Ongoing
Initiation date
2023-12-08
Report date
2024-06-12
Voluntary/Mandated
Voluntary: Firm initiated
Location
Denver, CO, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1942-2024