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Recall Observatory FDA recall evidence

Device product

Merge OrthoCase software. The firm name on the label is Merge Healthcare, Hartland, WI.

Z-0878-2017

October 08, 2015

Class II

Product summary

Firm
Merge Healthcare, Inc.
Event
Event 75909
Status
Terminated
Classification
Class II
Quantity
30 sites potentially have the effected versions
Official record key
device-enforcement:Z-0878-2017

Official wording

Reason: Measurements in the software are changing after saving a plan with a measurement result, which may result in potential patient injury or delay in diagnosis or treatment.

Code information: Versions: 2.0, 2.1, 2.1.1, 3.1, 3.2, 3.2.4, 3.3, 3.3.1, 3.4, 3.5.1, 3.5.1.1, 3.5.2, 3.5.3, 3.5.4, 3.5.5, 3.6, 3.6.1, 3.6.2, 3.7, 3.7.1, 3.7.2, 3.7.2 Vet, and 3.7.3

Distribution pattern: Distribution was made to medical facilities in CA, CO, CT, MA, MD, MN, MT, NE, NV, NY NJ, PA, SC, WA, and WI. Foreign distribution was made to Canada, as well as other countries.

Derived failure modes

  • Device software or design

    reason.device_software_design · v1.0.0

    software are changing after saving a plan with a measurement result, which may result in