Phadia Us recalls

Phadia Us appears in 9 official U.S. recall notices indexed by RecallRadar, most recently on 2023-07-05.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Phadia 2500EE instrument -Intended for the in vitro semi-quantitative measurement of IgG antibodies directed to gliadin in human serum or p…
  FDA Device · Class II · 2023-07-05 · Phadia Us
• EliA GliadinDP IgG Well in the Phadia 2500EE instrument (Material Number 12410002) EliA GliadinDP IgG is intended for the in vitro semi-qua…
  FDA Device · Class II · 2023-07-05 · Phadia Us
• EliA dsDNA Well - Product Usage: intended for the In-Vitro quantitative measurement of IgG antibodies directed to dsDNA in human serum and…
  FDA Device · Class II · 2021-02-17 · Phadia Us
• ImmunoCAP Allergen c6, Amoxicilloyl ( Article number 14-4451-016)
  FDA Device · Class II · 2018-04-11 · Phadia Us
• ImmunoCAP Allergen c5, Ampicilloyl (article number 14-4450-01)
  FDA Device · Class II · 2018-04-11 · Phadia Us
• Phadia 1000 Instrument, Article Number 12-3800-01
  FDA Device · Class II · 2018-01-24 · Phadia Us
• EliA Sample Diluent, Article number, 83-1023-01
  FDA Device · Class II · 2017-03-08 · Phadia Us
• Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versions since launch in 2003)
  FDA Device · Class II · 2015-01-21 · Phadia Us
• PHADIA Varelisa Cardiolipin IgM Cardiolipin autoantibody immunological test system (IgM class antibodies)
  FDA Device · Class III · 2012-09-05 · Phadia Us