Rappel de Electronic inflator IN-32-01- AKSI according to TU 9444-040-27507632-2009 in the following versions: type 1 with heated injection gas and supply of 32 l / min; type 2 without preheating of the injected gas and supplying 32 l / min; Type 3 with heated gas injection and supply of 20 l / min.

Russian data is current through January 2019. All of the data comes from the Federal Service for Surveillance in Healthcare, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Russia.

Manufacturer Recall