MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2024 - (Recall #: Z-2753-2024)

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 procedural kits labeled as: UMBILICAL LINE KIT W/FOAM, Pack Number DYNDL1588A

Product Classification:

Class II

Date Initiated: April 8, 2024

Date Posted: September 4, 2024

Recall Number: Z-2753-2024

Event ID: 94581

Reason for Recall:

Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that may pose a risk to patient health.

Status: Ongoing

Product Quantity:

Code Information:

DYNDL1588A , Lot Number 23ELA011 ; DYNDL1588A , Lot Number 23HLA426 ; DYNDL1588A , Lot Number 23JLA181 ; DYNDL1588A , Lot Number 24ALA515

Distribution Pattern:

Worldwide

Voluntary or Mandated:

Voluntary: Firm initiated