MEDLINE INDUSTRIES, LP - Northfield: Medical Device Recall in 2024 - (Recall #: Z-0514-2025)

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) NEURAXIAL KIT, REF PAIN1876A

Product Classification:

Class II

Date Initiated: October 16, 2024

Date Posted: December 4, 2024

Recall Number: Z-0514-2025

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: 360 units

Code Information:

Codes: 1) PAIN1876A UDI-DI: 10195327433666 (each) 40195327433667 (case), Lot Number: 23KLA330

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated