MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2025 - (Recall #: Z-1458-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

Medline medical procedure kits, containing Medtronic Aortic Root Cannula, labeled as follows: HEART BASIN PACK-LF

Product Classification:

Class I

Date Initiated: February 21, 2025

Date Posted: April 16, 2025

Recall Number: Z-1458-2025

Event ID: 96443

Reason for Recall:

Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.

Status: Ongoing

Product Quantity: 320 units

Code Information:

HEART BASIN PACK-LF, UDI/DI 10195327563561 (ea) 40195327563562 (case), Lot Numbers 24BMB798, 24DMH381, 24EMF949, 24GMF161, 24IMB237.

Distribution Pattern:

US: CA, FL, MN, NY, OH, OR, PA, TX, WV

Voluntary or Mandated:

Voluntary: Firm initiated