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FDAMarch 19, 2024device

Medtronic Vessel Cannulae: a) DLP¿ 2 mm Vessel Cannula Blunt Tip, Model Number 30004; b) DLP¿ 3 mm Vessel Cannula Blunt Tip, Model Number 30003

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

The hazard

Potential for unsealed sterile packing.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic perfusion systemsmedtronicmedtronic perfusion

UPCs

00613994646156006739781798412061399464615020613994646174

Recall history

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

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Medtronic Vessel Cannulae: a) DLP¿ 2 mm Vessel Cannula Blunt Tip, Model Number 30004; b) DLP¿ 3 mm Vessel Cannula Blunt Tip, Model Number 30003 — Recall Details · AllClear