Class II

Medical Device Recall: MEDLINE procedure kits labeled as follows: 1) NEURAXIAL KIT, REF PAIN1876A

MEDLINE INDUSTRIES, LP - Northfield · October 16, 2024

Reason for Recall

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

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

360 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0514-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.