Phadia Ab recalls

Phadia Ab appears in 5 official U.S. recall notices indexed by RecallRadar, most recently on 2024-01-31.

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

• EliA GBM Wells, Material Number 14551401, for Phadia 250, 2500, and 5000
  FDA Device · Class II · 2024-01-31 · Phadia Ab
• Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including software for immunodia…
  FDA Device · Class II · 2019-09-04 · Phadia Ab
• EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro quantitative measurement of IgM class rheum…
  FDA Device · Class II · 2019-07-10 · Phadia Ab
• Phadia Prime software, article number 12-4101-00, as used in combination with the Phadia 250 Instrument, article number 12-3900-01 and EliA…
  FDA Device · Class II · 2018-04-11 · Phadia Ab
• EliA SmDP Well, Article Number 14-5624-01 Product Usage: EliA SmDP is intended for the in vitro semi-quantitative measurement of IgG antibo…
  FDA Device · Class II · 2016-02-03 · Phadia Ab