FDA Enforcement Class II Ongoing

epoc NXS Host Blood Analysis System, Siemens Material Numbers 11413497 (EU), 11413475 (US), 11413506 (CA), 11413517 (MX), 11413518 (ROW), 11413498 (JP), 11413583 (CN, KR), 11413879 (IN) with software versions from 4.9.4 to the current version 4.11.11

Recall: Z-0601-2024 · Reported December 27, 2023

Enforcement

Recall Number
Z-0601-2024
Event ID
93388
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Siemens Healthcare Diagnostics Inc
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
December 27, 2023
Initiation Date
October 19, 2023
Classification Date
December 20, 2023
Address
2 Edgewater Dr, N/A, Norwood, MA, 02062-4637, United States

Description

epoc NXS Host Blood Analysis System, Siemens Material Numbers 11413497 (EU), 11413475 (US), 11413506 (CA), 11413517 (MX), 11413518 (ROW), 11413498 (JP), 11413583 (CN, KR), 11413879 (IN) with software versions from 4.9.4 to the current version 4.11.11

Reason

Siemens Healthcare Diagnostics Inc. has confirmed a potential issue that could occur under certain conditions, a software problem is causing erroneous results to be printed. When the results are run on the epoc NXS Host and Delete Blood Tests feature is enabled, the results that are generated at the time of testing are correct; however, when this issue occurs, results that are printed, saved and/or transferred to a data manager, may include unselected analytes that are from a previous patient or QC test. The worst possible outcome may result in a failure to diagnose hyperkalemia, due to an erroneous depressed potassium level or inappropriate treatment to hyperglycemia due to erroneous glucose reading.

Code Info

UDI-DI: 00630414605760 00630414606095 00630414605821 00630414605838 00630414605678 00630414605814 00630414612447 00630414631028; All serial numbers.

Distribution

US Nationwide. Global Distribution.

Quantity

10,183 devices