MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2025 - (Recall #: Z-1708-2025)

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 procedure kits, labeled as: NON STERILE I&D KIT, REF DYKM1438

Product Classification:

Class II

Date Initiated: March 19, 2025

Date Posted: May 7, 2025

Recall Number: Z-1708-2025

Event ID: 96630

Reason for Recall:

It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.

Status: Ongoing

Product Quantity: 240 units

Code Information:

UDI/DI 10889942529964 (EA) 40889942529965 (CS), Lot Numbers: 23KDB283

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Panama and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated