MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2024 - (Recall #: Z-0510-2025)

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 procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20

Product Classification:

Class II

Date Initiated: October 16, 2024

Date Posted: December 4, 2024

Recall Number: Z-0510-2025

Event ID: 95615

Reason for Recall:

The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.

Status: Ongoing

Product Quantity: 5975 units

Code Information:

Codes: 1) EPICATH19, UDI/DI 10889942358311(each) 40889942358312(case), Lot Numbers: 22FBX111, 22FBY472, 23FBT886, 23GBL403, 23GBO700, 23GBO701, 23GBO702; 2) EPICATH20, UDI-DI: 10889942358328 (each) 40889942358329 (case), Lot Numbers: 22FBN457, 22HBM699, 22HBN345, 23CBF321, 23DBM670, 23FBK248, 23GBO703, 23GBO704 23GBO705, 23KBG553, 23KBS111

Distribution Pattern:

US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands

Voluntary or Mandated:

Voluntary: Firm initiated