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Recall Observatory FDA recall evidence

Device product

Ingenuity Core 128 Computed Tomography X-ray Systems, Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes

Z-1355-2016

February 05, 2016

Class II

Product summary

Firm
Philips Medical Systems (Cleveland) Inc
Event
Event 73338
Status
Terminated
Classification
Class II
Quantity
174 Units
Official record key
device-enforcement:Z-1355-2016

Official wording

Reason: The firm was notified of a software error in which the system may not automatically send all image/data series to remote devices.

Code information: Model No. 728323; S/N: 30016, 30023, 30151, 30153, 32000, 32001, 32008, 32012, 32042, 32044, 32057, 32061, 32065, 32067, 32068, 32069, 32076, 32100, 32106, 32138, 32139, 32140, 32141, 32142, 32143, 32144, 32145, 32146, 32147, 32148, 32149, 32150, 32151, 32152, 32153, 32154, 32155, 32156, 32157, 32158, 32159, 32160, 32161, 32162, 32163, 32164, 32165, 32166, 32167, 52023, 52028, 52049, 320001, 320003, 320006, 320008, 320010, 320024, 320026, 320029, 320031, 320037, 320054, 320070, 320078 320090, 320092, 320107, 320202, 320207, 320224, 320225, 320226, 320227, 320228, 320229 320230, 320231, 320232, 320233, 320234, 320235, 320236, 320238, 320239, 320240, 320241, 320242, 320243, 320245, 320246, 320247, 320248, 320250, 320251, 320252, 320254, 320255, 320256, 320258, 336011, 336012, 336015, 336016, 336018, 336025, 336027, 336028, 336029, 336034, 336040, 336044, 336068, 336072, 336076, 336092, 336100, 336102, 336104, 336142, 336148, 336149, 336150, 336151, 336152, 336153, 336154, 336155, 336156, 336157, 336158, 336159, 336160, 336161, 336162, 336163, 336164, 336166, 336167, 336168, 336170, 336171, 336172, 336173, 336174, 336175, 336176, 336177, 336178, 336180, 336181, 336182, 336183, 336184, 336185, 336186, 336188, 336190, 336192, 336193, 336194, 30035, 320257, 333047, 336165, 336179, 336187, 336189, 336191, 336195, 336196, 336197, 336199 & 336200.

Distribution pattern: Worldwide Distribution - US to the District of Columbia: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA & WV. Product was also shipped to the following countries: Afghanistan, Australia, Austria, Bangladesh, Belgium, Brazil, Canada, China, Cuba, Denmark, Egypt, Ethiopia, Finland, France, Germany, Ghana, Gibraltar, Greece, Hungary, Iceland, India, Indonesia, Iran, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kyrgyzstan, Lebanon, Lithuania, Macedonia, Malawi, Mexico, Myanmar, Netherlands, New Zealand, Norway, Oman, Palestinian, Philippines, Poland, Republic of Korea, R¿union, Romania, Russian Federation, Singapore, Spain, Sweden, Switzerland, Taiwan, Thailand, Ukraine, United Arab Emirates, United Kingdom, Uzbekistan & Viet Nam.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software error