MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2024 - (Recall #: Z-0123-2025)

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:

MEDLINE KIT CV I II, REF DYNJ906071B

Product Classification:

Class II

Date Initiated: August 28, 2024

Date Posted: October 23, 2024

Recall Number: Z-0123-2025

Event ID: 95393

Reason for Recall:

Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.

Status: Ongoing

Product Quantity: 56 kits

Code Information:

UDI/DI 40195327227235 (case), 10195327227234 (each), Lot Numbers: 24ABA223

Distribution Pattern:

US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated