FDA recall record

Siemens Healthcare Diagnostics ADVIA Chemistry XPT System, Siemens Material Number 10723034 recall — FDA Z-1399-2015

Siemens Healthcare Diagnostics has confirmed an issue with ADVIA Chemistry XPT software version 1.0.2. The system may cause samples to remain in an…

Class IIclassification
Z-1399-2015official record ID
Apr 15, 2015report date

Recall record at a glance

Official recordZ-1399-2015
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSiemens Healthcare Diagnostics, Inc.
Report dateApr 15, 2015
Recall initiation dateFeb 11, 2015
Quantity16 units: 3 Domestic, 13 Foreign
LocationTarrytown, NY, United States

Official product description

ADVIA Chemistry XPT System, Siemens Material Number 10723034, Software Version 1.0.2, Siemens Material Number 11219493, IVD. The ADVIA XPT Chemistry System is an automated, clinical chemistry analyzer that runs tests on serum, plasma, urine, or cerebral spinal fluid in random access and batch modes at a throughput rate of both 1800 photometric tests per hour and 600 electrolyte (ISE) tests per hour.

Why the product was recalled

Siemens Healthcare Diagnostics has confirmed an issue with ADVIA Chemistry XPT software version 1.0.2. The system may cause samples to remain in an Inprocess state. Test results on a sample that is held Inprocess will not transmit to the LIS. Manual intervention is necessary to complete the processing of the samples that are held Inprocess.

Distribution information

Distributed in the states of AZ, CA, and WA, and the countries of Germany, Italy, Spain, and UK.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

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

What to do next

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