Phadia US Inc: Medical Device Recalls in 2023

Updated on March 25, 2026.

According to to data from the FDA, there were 2 medical device recalls made by Phadia US Inc in 2023. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Phadia 2500EE instrument -Intended for the in vitro semi-quantitative measurement of IgG antibodies directed to gliadin in human serum or plasma (Li-heparin, EDTA) to aid in the diagnosis of celiac disease Material Number 12410002
EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Number 12410002) EliA GliadinDP IgG is intended for the in vitro semi-quantitative measurement of IgG antibodies directed to gliadin in human serum or plasma (Li-heparin, EDTA) to aid in the diagnosis of celiac disease Material Number 14553901