MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2025 - (Recall #: Z-1590-2025)

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 Convenience kits used for various procedures: 1) ANGIO CONSOLIDATED PACK, Model Number: DYNJHTCAD1; 2) ANGIOGRAPHY TRAY-LF, Model Number: DYNJ05350V; 3) ANGIOGRAPHY PACK, Model Number: DYNJ38144C

Product Classification:

Class II

Date Initiated: March 3, 2025

Date Posted: April 23, 2025

Recall Number: Z-1590-2025

Event ID: 96510

Reason for Recall:

There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.

Status: Ongoing

Product Quantity: 2,118 units

Code Information:

1) DYNJHTCAD1, UDI-DI: 10888277087583(each), 40888277087584(case), Lot Number: 24JBS743; 2) DYNJ05350V, UDI-DI: 10193489316629(each), 40193489316620(case), Lot Number: 24JBU500; 3) DYNJ38144C, UDI-DI: 10193489854916(each), 40193489854917(case), Lot Number: 24KBD294

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Canada, Mexico, Panama, Virgin Islands.

Voluntary or Mandated:

Voluntary: Firm initiated