Recall Z-0512-2025— MEDLINE INDUSTRIES, LP - Northfield

Name: FDA recall Z-0512-2025
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. FDA's recall record names no specific 510(k) clearance for this event. Product: MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL, REF PAIN1423A; 2) CONT. 20G EPI MRI COMPATIBLE, REF PAIN1470A; 3) EPIDURAL CATHETERIZATION KIT, REF PAIN1644. 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

Product description

MEDLINE procedure kits labeled as follows: 1) PERIPHERAL CONTINUOUS NERVE BL, REF PAIN1423A; 2) CONT. 20G EPI MRI COMPATIBLE, REF PAIN1470A; 3) EPIDURAL CATHETERIZATION KIT, REF PAIN1644

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.