FDAFDA · Food and drugs·Recall number Z-0508-2025
MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector
Published December 4, 2024 · Recall initiated: October 16, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- MEDLINE INDUSTRIES, LP - Northfield
- Distributor
- US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands
- Lot
- UDI/DI 10193489490312 (each), 40193489490313 (case), Lot Numbers: 21ABD173, 21EBC720, 21GBG632, 21HBF316, 21IBH392, 21IBM516, 21JBJ902, 21JBP187, 22IBL115, 22KBD213, 22OBI434, 23ABA553, 23ABO991, 23BBG757, 23CBO551, 23EBT535
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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