FDAMay 10, 2024device

Medtronic Ascenda Intrathecal Catheter, Models: a) 8780 (114 cm); b) 8781 (140 cm); c) 8784 (catheter pump revision kit)

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Design update to the Ascenda Intrathecal Catheter Models 8780, 8781, and 8784. The intent of the design update is to reduce the potential for tissue growth into the Ascenda catheter connector which may potentially lead to catheter occlusion.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic neuromodulationmedtronic

UPCs

00643169202122

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Medtronic Ascenda Intrathecal Catheter, Models: a) 8780 (114 cm); b) 8781 (140 cm); c) 8784 (catheter pump revision kit) — Recall Details · AllClear