FDA recall Z-0362-2020

Tec Com Gmbh · Class II · device

Product

TECOTHERM NEO, 100-130/200-240 VAC, 50-60 Hz/ max. 350VA, Class I, Schutzklasse I IP 20, UDI: 04260498580002 - Product Usage: The Thermo-Regulation System TECOTHERM NEO is designed for controlled cold & heat treatment procedures. By means of a mattress, cold and heat is provided to the patient, depending on the therapy objective.

Reason for recall

The action is being initiated due to potential installation of faulty peltier-elements within the thermo-regulation system. Failure of the peltier-element would report a system failure and no longer be able to guarantee temperature control at full power.

Distribution

US Nationwide distribution in the state of UT.

Key facts

Status
Terminated
Initiation date
2018-08-14
Report date
2019-11-20
Termination date
2019-12-20
Voluntary/Mandated
Voluntary: Firm initiated
Location
Kabelsketal, N/A, Germany

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0362-2020