MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2023 - (Recall #: Z-1065-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

FEMORAL ARTERY PACK-LF. Sterile Procedural Tray

Product Classification:

Class II

Date Initiated: November 17, 2022

Date Posted: February 15, 2023

Recall Number: Z-1065-2023

Event ID: 91386

Reason for Recall:

Sterile blades within sterile kits have the potential for the blade to puncture the outer foil layer of the sterile packaging.

Status: Ongoing

Product Quantity: 15 cases (30 units)

Code Information:

Item Number: DYNJ0826625Q, Case UDI/GTIN: 40193489377942, Unit UDI/GTIN: 10193489377941, Lot Number: 22KMA163, 22JME722

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Canada, Japan, Mexico, Panama, Turks & Caicos, United Arab Emirates.

Voluntary or Mandated:

Voluntary: Firm initiated