FDA recall Z-1091-2022

Neuralynx Inc · Class II · device

Product

ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology System. CAUTION--INVESTIGATIONAL DEVICE Limited by Federal (or United States) law to investigational use. Only for use in Non-Significant Risk studies under the supervision of an IRB.

Reason for recall

Atlas Stim Headbox (ASHB) was delivered to US customers under a premise that the device had an Investigational Device Exemption (IDE) and was for research use only, but the manufacturer does not have an approved IDE by the FDA. The product has not undergone electrical safety testing and has not received regulatory clearance.

Distribution

U.S. Nationwide distribution in the states of AL, CA, IL, MN, NC, RI.

Key facts

Status
Ongoing
Initiation date
2022-03-14
Report date
2022-05-25
Voluntary/Mandated
Voluntary: Firm initiated
Location
Bozeman, MT, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1091-2022