Home / Recalls / Medical Devices
Ivenix, Inc. recalls Ivenix Infusion System (IIS)
Recalled July 20, 2022 · FDA recall Z-1381-2022 · Ivenix
Hazard
Downstream occlusion alarm is sometimes immediately followed by a pump problem alarm. · FDA Class II
Units
1335 devices
Sold at
US Nationwide distribution in the states of NJ and WI.
Description
Downstream occlusion alarm is sometimes immediately followed by a pump problem alarm.
Product
Ivenix Infusion System (IIS)
Manufacturer(s)
Ivenix, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →