Siemens Healthcare Diagnostics, Inc recalls ADVIA Centaur iPTH Calibrator 2 pk; REF 10492394. For in vitro diagnostic use in calibrating Intact PTH assays.

Recalled June 12, 2013 · FDA recall Z-1514-2013 · Siemens Healthcare Diagnostics

Hazard

iPTH Assay- reagent and calibrator lots may have demonstrated higher than anticipated variability · FDA Class II

Units

99 (2 pk)

Sold at

Nationwide Distribution.

Description

iPTH Assay- reagent and calibrator lots may have demonstrated higher than anticipated variability

Product

ADVIA Centaur iPTH Calibrator 2 pk; REF 10492394. For in vitro diagnostic use in calibrating Intact PTH assays.

Manufacturer(s)

Siemens Healthcare Diagnostics, Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →