Medline recalls Nexus 19/20G catheter connectors with specific lot numbers due to potential failure to insert catheters correctly. Affected units may need adjustment or replacement.
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Medline is recalling its Nexus 19/20G catheter connectors because they might not allow catheters to be inserted properly if not fully open. This could lead to improper catheter placement, which may cause complications during medical procedures.
The catheter connectors may not stay fully open, making it difficult to insert catheters as intended. This could result in improper catheter placement during medical procedures, potentially causing complications.
Healthcare professionals using catheter connectors for medical procedures are most likely affected. Patients receiving catheter treatments could be at risk if the connector fails to insert correctly.
Check for lot numbers 21ABD173, 21EBC720, 21GBG632, 21HBF316, 21IBH392, 21IBM516, 21JBJ902, 21JBP187, 22IBL115, 22KBD213, 22OBI434, 23ABA553, 23ABO991, 23BBG757, 23CBO551, 23EBT535 on the packaging or label.
Ensure the connector is fully open before attempting catheter insertion.
Lot numbers 21ABD173, 21EBC720, 21GBG632, 21HBF316, 21IBH392, 21IBM516, 21JBJ902, 21JBP187, 22IBL115, 22KBD213, 22OBI434, 23ABA553, 23ABO991, 23BBG757, 23CBO551, 23EBT535.
Check the lot number on the packaging or label; affected units have specific lot numbers listed in the recall notice.
The recall does not require stopping use; healthcare professionals should ensure the connector is fully open before insertion.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0508-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0508-2025 from Medline. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
