Medtronic Perfusion Systems: Medical Device Recall in 2024 - (Recall #: Z-1796-2024)

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 I.M.A. Cannulae: DLP¿ 1 mm Arteriotomy Cannula, Model Number 31001

Product Classification:

Class II

Date Initiated: March 19, 2024

Date Posted: May 22, 2024

Recall Number: Z-1796-2024

Event ID: 94274

Reason for Recall:

Potential for unsealed sterile packing.

Status: Ongoing

Product Quantity: 7935 units

Code Information:

GTIN 00613994575319, Lot Numbers: 2023041320, 2023041323; GTIN 00673978180465, Lot Numbers: 2023041316, 2023041323; GTIN 20613994575313, Lot Numbers: 2023041316, 2023041318, 2023041320, 2023041323, 202305C146, 202305C154

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated