MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector
- Recall date
- October 16, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0508-2025
- 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 NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector
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