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FDA (Device enforcement)Recalled 2024-01-26class ii

Ortho-Clinical Diagnostics, Inc.: VITROS XT 7600 Integrated System, Catalog No. 6844461

Hazard

A software defect affecting VITROS Systems running VITROS Software Versions 3.8.0 and 3.8.1 causes the Configurable Westgard Rules to not report as expected. When a new control is defined, configurable Westgard rules, if selected, are not flagged or reported with the applicable QC results if the statistical criteria is met. This may result in acceptance of QC results that do not meet acceptance criteria, which may cause erroneous patient results to be reported.

Details from the source

Reason for recall: A software defect affecting VITROS Systems running VITROS Software Versions 3.8.0 and 3.8.1 causes the Configurable Westgard Rules to not report as expected. When a new control is defined, configurable Westgard rules, if selected, are not flagged or reported with the applicable QC results if the statistical criteria is met. This may result in acceptance of QC results that do not meet acceptance criteria, which may cause erroneous patient results to be reported. Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Denmark, France, Germany, India, Italy, Japan, Mexico, Norway, Portugal, Russia, Singapore, Spain, Sweden, The Netherlands, United Kingdom. Quantity: 142 US; 78 OUS Lot/code info: VITROS System Software Versions 3.8.0 or 3.8.1 UDI-DI 10758750031610 Serial Numbers: US: J76000050 J76000878 J76001555 J76000108 J76000905 J76001558 J76000144 J76000909 J76001559 J76000148 J76000922 J76001565 J76000179 J76000930 J76001570 J76000192 J76000968 J76001577 J76000195 J76001106 J76001581 J76000199 J76001171 J76001583 J76000200 J76001172 J76001589 J76000206 J76001206 J76001592 J76000207 J76001207 J76001595 J76000208 J76001218 J76001596 J76000241 J76001230 J76001597 J76000298 J76001231 J76001599 J76000313 J76001232 J76001600 J76000317 J76001234 J76001611 J76000324 J76001235 J76001616 J76000333 J76001239 J76001617 J76000342 J76001260 J76001620 J76000352 J76001263 J76001638 J76000353 J76001270 J76001639 J76000420 J76001274 J76001643 J76000422 J76001292 J76001644 J76000456 J76001293 J76001647 J76000459 J76001294 J76001648 J76000460 J76001331 J76001650 J76000468 J76001340 J76001652 J76000495 J76001351 J76001659 J76000502 J76001357 J76001660 J76000524 J76001370 J76001666 J76000525 J76001376 J76001667 J76000537 J76001383 J76001668 J76000561 J76001384 J76001669 J76000609 J76001385 J76001671 J76000709 J76001392 J76001674 J76000743 J76001404 J76001675 J76000747 J76001406 J76001678 J76000783 J76001516 J76001679 J76000790 J76001517 J76001687 J76000803 J76001518 J76001692 J76000805 J76001519 J76001700 J76000806 J76001520 J76001703 J76000817 J76001535 J76001705 J76000862 J76001540 J76001711 J76000866 J76001549 J76001714 J76000868 J76001552 J76001748 J76000871 J76001553 J76001879 J

UPC codes

10758750031610

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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