FDAJanuary 30, 2024device

MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-776

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

The hazard

Non-conformance may prevent the guidewire from passing through the introducer hub during a surgical procedure. The inability of the guidewire to pass through the introducer is due to the presence of voids in the internal lumen of the sheath hub, potential risk of the non-conformance is a delay in procedure, wherein the user may need to exchange the sheath to complete the case

What to do

FDA enforcement status: Ongoing

Brands named

angiodynamics

UPCs

15051684023191

Recall history

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

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