FDA recall record

Siemens Healthcare Diagnostics ADVIA Centaur Calibrator A recall — FDA Z-1970-2013

Calibrator A lot CA77 is under-recovering to the assigned target for the ADVIA Centaur Total T4 Assay.

Class IIIclassification
Z-1970-2013official record ID
Aug 21, 2013report date

Recall record at a glance

Official recordZ-1970-2013
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmSiemens Healthcare Diagnostics, Inc.
Report dateAug 21, 2013
Recall initiation dateJun 28, 2013
Quantity265 Cal A 6 packs (US and OUS)
LocationEast Walpole, MA, United States

Official product description

ADVIA Centaur Calibrator A. Cat. #04800735, SMN 10285904 (6 pack); Cat. # 04800840, SMN 10285905 (6 pack - REF). For calibrating the following assays using the ADVIA Centaur or ACS:180 systems: FT3, T3, T4, Tup, FT4, THEO2.

Why the product was recalled

Calibrator A lot CA77 is under-recovering to the assigned target for the ADVIA Centaur Total T4 Assay.

Distribution information

Worldwide Distribution-Nationwide including PR and the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, NC, NJ, NV, NY, OH, PA, TN, TX, VA, VT, and WV and the countries of Slovakia, Germany, Turkey, TW, HK, CH, TH, BR, CN, SG, and ZA.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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