ClearanceBrief
Recall Z-0972-04 ยท DHX System, Test, Carcinoembryonic Antigen

Diagnostic Products Corp

Immulite 1000 CEA Catalog No. LKCE1

DateJul 20, 2004 (initiated May 3, 2004)
StatusTerminated
ReasonInstabililty
Root causeOther
ActionNotice was made via email or telephone. Users are to discard kits.
Quantity884
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K970877IMMULITE CEA
Diagnostic Products Corp., Sep 22, 1997