Atlas FDA

Phadia US Inc

7 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch Phadia US Inc

RecordFirmDate
EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Number 12410002) EliA Gl recall (Z-2040-2023)Phadia US Inc2023-06-30
Phadia 2500EE instrument -Intended for the in vitro semi-quantitative measurement of IgG a recall (Z-2041-2023)Phadia US Inc2023-06-30
EliA dsDNA Well - Product Usage: intended for the In-Vitro quantitative measurement of IgG recall (Z-1107-2021)Phadia US Inc2021-02-11
EliA Sample Diluent, Article number, 83-1023-01 recall (Z-1253-2017)Phadia US Inc2017-02-24
Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instru recall (Z-0947-2015)Phadia US Inc2015-01-12
PHADIA Varelisa Cardiolipin IgM Cardiolipin autoantibody immunological test system (IgM cl recall (Z-2285-2012)Phadia US Inc2012-08-28
ImmunoCAP Allergen Ri206, Cockroach American, Periplaneta americana It is an analyte speci recall (Z-1055-2012)Phadia US Inc2012-02-17

Track Phadia US Inc automatically

Every clearance here is in the API, with alerts when new ones post.