Z-0508-2025 Class II Ongoing
FDA device recall Z-0508-2025 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Oct 16, 2024 and is designated Class II. Reason for recall: The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position. The recall status is ongoing. Affected quantity: 1975 units.
Recall Details
- Product Type
- Devices
- Report Date
- Dec 4, 2024
- Initiation Date
- Oct 16, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1975 units
Product Description
MEDLINE NEXUS 19/20G CATH CONNECTOR, Medline SKU REF NEXCONNECT, Catheter Connector
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 Pattern
US Nationwide. Bermuda, Canada, Panama, UAE, US Virgin Islands
Code Information
UDI/DI 10193489490312 (each), 40193489490313 (case), Lot Numbers: 21ABD173, 21EBC720, 21GBG632, 21HBF316, 21IBH392, 21IBM516, 21JBJ902, 21JBP187, 22IBL115, 22KBD213, 22OBI434, 23ABA553, 23ABO991, 23BBG757, 23CBO551, 23EBT535
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0508-2025
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026