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FDAFDA · Food and drugs·Recall number Z-1799-2024

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

Published May 22, 2024 · Recall initiated: March 19, 2024

Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Potential for unsealed sterile packing.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Medtronic Perfusion Systems
Distributor
Worldwide distribution.
Lot
a) Model Number 30004, GTIN 00613994646156, Lot Numbers: 2023041305; a) Model Number 30004, GTIN 00673978179841, Lot Numbers: 2023041300; a) Model Number 30004, GTIN 20613994646150, Lot Numbers: 2023041300, 2023041305, 202306C194; b) Model Number 30003, GTIN 20613994646174, Lot Numbers: 2023041298, 202306C221
Risk classification
Class II
Area (FDA)
device
Country
United States

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