Recall Z-0508-2025— MEDLINE INDUSTRIES, LP - Northfield

Name: FDA recall Z-0508-2025
Creator: U.S. Food and Drug Administration
Published: 2024-10-16

Class II · Ongoing

Class II FDA medical device recall by MEDLINE INDUSTRIES, LP - Northfield, initiated 2024-10-16. It names one FDA 510(k) clearance: K051171. Product: MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector. Reason: The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position..

Recalling firm: MEDLINE INDUSTRIES, LP - Northfield
Classification: Class II
Status: Ongoing
Initiated: 2024-10-16
Firm location: Northfield, IL, United States

510(k) clearances named in this recall

1 on FDA's record

K051171 — STINGRAY EPIDURAL CATHETER CONNECTOREpimed International, Inc.·cleared 2005-08-26

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.