Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0320-2024 — Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device, Model Number MUS0130069X6

U.S. FDA — Device Enforcement · United States · 2023-10-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0320-2024
Date of alert
2023-10-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
08033477090719
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.