Event Medical Inspiration Ventilator System, i Series and LS 12.1 LCD recall — FDA Z-0230-2016
A component on the systems power board can fail in a manner which can cause the ventilator to shut down without alarming.
Overview of recall records associated with Event Medical LTD, including dates, categories and classifications where available.
Classification mix: Class I: 1.
A component on the systems power board can fail in a manner which can cause the ventilator to shut down without alarming.
This page summarizes recall records in which the official source identifies Event Medical LTD as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.