Class II
Medical Device Recall: MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20
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
5975 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0510-2025
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.