Medtronic Perfusion Systems: Medical Device Recall in 2024 - (Recall #: Z-1799-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 19, 2024

Date Posted: May 22, 2024

Recall Number: Z-1799-2024

Event ID: 94274

Reason for Recall:

Potential for unsealed sterile packing.

Status: Ongoing

Product Quantity: 5719 units

Code Information:

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

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated