Medtronic Perfusion Systems: Medical Device Recall in 2024 - (Recall #: Z-1795-2024)

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 DLP Coronary Ostial Cannulae, Model Number 30050

Product Classification:

Class II

Date Initiated: March 19, 2024

Date Posted: May 22, 2024

Recall Number: Z-1795-2024

Event ID: 94274

Reason for Recall:

Potential for unsealed sterile packing.

Status: Ongoing

Product Quantity: 250 units

Code Information:

GTIN 00613994576019, Lot Numbers: 2023070529; GTIN 20613994576013, Lot Numbers: 2023070529

Distribution Pattern:

Worldwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated