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Recall Observatory FDA recall evidence

Device product

Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 Intended for use as a primary diagnostic and analysis tool for diagnostic images.

Z-1045-2017

December 16, 2016

Class II

Product summary

Firm
DICOM GRID INC
Event
Event 76187
Status
Terminated
Classification
Class II
Quantity
209
Official record key
device-enforcement:Z-1045-2017

Official wording

Reason: A software error caused the window/level to become the same in one series regardless if the image had different levels; image results have a washed-out grey appearance.

Code information: Unavailable

Distribution pattern: U.S. distribution to the following; TX, FL, NE, CA, WI, AZ, NH, MO, MA, CO, PA, NV, PR, IL, OH, NY, MD, NJ, MN, MI, CT, VA, GA, UT, KS, WA, MI, HI. Foreign distribution to the following; Canada, Spain, Israel, Singapore, Kosovo, Austria, Brazil, Malaysia, Australia.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software error