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Recall Observatory FDA recall evidence

Device product

Ingenuity Core128/Elite China 728324

Z-2277-2018

March 28, 2018

Class II

Product summary

Firm
Philips Medical Systems (Cleveland) Inc
Event
Event 80176
Status
Terminated
Classification
Class II
Quantity
Unavailable
Official record key
device-enforcement:Z-2277-2018

Official wording

Reason: A problem has been detected in the X-Ray Tube. The affected tubes have a production defect that allows oil leakage from the tube housing, if it were to re-occur, could pose a risk for patients or users.

Code information: UDI: (01)00884838059863(21)336856, Serial Number: 336856; UDI: (01)00884838059863(21)336851, Serial Number: 336851; UDI: (01)00884838059863(21)336849, Serial Number: 336849; UDI: (01)00884838059863(21)336852, Serial Number: 336852; UDI: (01)00884838059863(21)336853, Serial Number: 336853; UDI: (01)00884838059863(21)336855, Serial Number: 336855; UDI: (01)00884838059863(21)336854, Serial Number: 336854; UDI: (01)00884838059863(21)336850, Serial Number: 336850

Distribution pattern: The systems were distributed to the following US states: HI, KS, and MO. The systems were distributed to the following foreign countries: Algeria, Austria, Brazil, China, Indonesia, Japan, Kenya, Korea, Mexico, Poland, Turkey, and Uganda.

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    production defect