Medical Devices Type II Updated 2021-11-25

ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)

Recalled Product

ALLURA XPER FD10 and FD20/10 (PRODUCT OF ALLURACLARITY FAMILY)


Hazard / Issue

Software defect

Issued by

Medical devices

View official government recall

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