Medical device recalls Moderate risk

MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE…

Recall date
October 16, 2024
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0510-2025
FDA classification
Class II
Brand / firm
MEDLINE INDUSTRIES, LP - Northfield
Sold / distributed
US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

MEDLINE procedure kits labeled as follows: 1) 20G EPI CATH SINGLE STERILE, REF EPICATH19 2) 20G EPI CATH SINGLE STERILE, REF EPICATH20

Get recall alerts

Free email alert whenever MEDLINE INDUSTRIES, LP - Northfield has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: MEDLINE INDUSTRIES, LP - Northfield