Phadia Us Inc
Portage, MI
This page shows every FDA and USDA recall linked to Phadia Us Inc. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
10
Total Recalls
2012
First Recall
2023
Most Recent
Phadia 2500EE instrument -Intended for the in vitro semi-quantitative measurement of IgG antibodies directed t...
Jun 30, 2023
· Device
Active
EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Number 12410002)
EliA GliadinDP IgG is inten...
Jun 30, 2023
· Device
Active
EliA dsDNA Well - Product Usage: intended for the In-Vitro quantitative measurement of IgG antibodies directed...
Feb 11, 2021
· Device
Terminated
ImmunoCAP Allergen c6, Amoxicilloyl ( Article number 14-4451-016).
ImmunoCAP Specific IgE is an in vitro quan...
Dec 18, 2017
· Device
Terminated
ImmunoCAP Allergen c5, Ampicilloyl (article number 14-4450-01).
ImmunoCAP Specific IgE is an in vitro quantit...
Dec 18, 2017
· Device
Terminated
Phadia 1000 Instrument, Article Number 12-3800-01.
Jul 5, 2017
· Device
Terminated
EliA Sample Diluent, Article number, 83-1023-01
Feb 24, 2017
· Device
Terminated
Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versio...
Jan 12, 2015
· Device
Terminated
PHADIA Varelisa Cardiolipin IgM
Cardiolipin autoantibody immunological test system (IgM class antibodies)
Aug 28, 2012
· Device
Terminated
ImmunoCAP Allergen Ri206, Cockroach American, Periplaneta americana
It is an analyte specific reagent and no...
Feb 17, 2012
· Device
Terminated