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Recall Observatory FDA recall evidence

Device product

Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device, Model Number MUS0130069X6

Z-0320-2024

October 12, 2023

Class II

Product summary

Firm
Medtronic Inc
Event
Event 93258
Status
Ongoing
Classification
Class II
Quantity
2767 units
Official record key
device-enforcement:Z-0320-2024

Official wording

Reason: The Mo.Ma Ultra device manifold is labelled with 2 stickers, an inferior and superior sticker, one on each side of the manifold. These stickers label the common carotid artery (CCA) proximal balloon and external carotid artery (ECA) distal balloon inflation and deflation ports. Both sides of the complaint units manifold were labelled with the superior label leading to an incorrect identification of the proximal and distal inflation /deflation ports when viewing the devices from the inferior side.

Code information: UDI/DI 08033477090719: UDI/DI 00763000451691

Distribution pattern: Worldwide distribution - US Nationwide and the countries of Algeria, Armenia, France, Germany, Iraq, Italy, Japan, Netherlands, Poland, Romania, Spain, Sweden, Switzerland, United Kingdom.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    label leading to an incorrect