FDA recall Z-2353-2026

Micromed S.p.A. · Class II · device

Product

SD LTM 64 PLUS, EEG Amplifier/recorder, Model/Catalog Number: SD LTM 64 PLUS, Software Version: firmware 2021.02, 2022.01 or 2022.02

Reason for recall

Natus has become aware of two complaints related to the SD LTM 64 PLUS where the EEG traces acquired from two or four different amplifiers used in a multiple amplifier configuration (128 or 256 channels) running firmware version 2022.02 were displayed with a shift of 1 second between the 64channels blocks. In rare circumstances, a fixed 1-second temporal delay may appear between two 64-channel modules with firmware 2021.02, 2022.01 or 2022.02 in a multi-module SEEG configuration, potentially leading to misinterpretation of results.

Distribution

Worldwide - US Nationwide distribution in the states of FL, PA.

Key facts

Status
Ongoing
Initiation date
2026-05-04
Report date
2026-06-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Mogliano Veneto, N/A, Italy

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2353-2026