Phadia AB

7 devices · 2 adverse event reports · 6 devices named in recalls

Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.

• Phadia 1000 12-3800-01

  SYSTEM, TEST, RADIOALLERGOSORBENT (RAST) IMMUNOLOGICAL
  1 recall1 report
• EliA GBM Well DECC055140

  Devices, measure, antibodies to glomerular basement membrane (gbm)
  1 recall0 reports
• EliA GliadinDP IgG Well DECC055390

  Antibodies, gliadin
  1 recall0 reports
• EliA RF IgM Well DECC056000

  SYSTEM, TEST, RHEUMATOID FACTOR
  1 recall0 reports
• EliA dsDNA Well DECC055000

  ANTI-DNA ANTIBODY, ANTIGEN AND CONTROL
  1 recall0 reports
• Phadia 2500EE 12-4100-02

  ANTIBODIES, ANTI-CYCLIC CITRULLINATED PEPTIDE (CCP)
  1 recall0 reports
• ImmunoCAP Allergen f202, Cashew nut 14-4835-01

  SYSTEM, TEST, RADIOALLERGOSORBENT (RAST) IMMUNOLOGICAL
  1 report