Medline recalls NEURAXIAL KIT PAIN1876A due to potential catheter insertion issues if connector isn't fully open. Affected kits have specific model and lot numbers.
The connectors may not allow catheters to be inserted as intended if the connector is not in the fully open position.
Medline is recalling NEURAXIAL KIT PAIN18:76A procedure kits because the connectors might not allow catheters to be inserted properly if not fully open. This could lead to improper medical procedures if the kit is used without checking the connector position.
The connectors in these kits may not stay in the fully open position, which can prevent catheters from being inserted correctly. This could lead to improper medical procedures if the kit is used without ensuring the connector is fully open.
Healthcare professionals using Medline NEURAXIAL KIT PAIN1876A procedure kits are most at risk. The recall affects kits sold with specific model numbers and lot numbers.
Check for the model number PAIN1876A on the kit label. Kits with lot number 23KLA330 are affected. These kits were sold with specific UDI-DI codes.
Ensure the connector is fully open before attempting catheter insertion to prevent improper insertion.
The recalled model is NEURAXIAL KIT PAIN1876A.
Lot number 23KLA330 is affected.
Check for the model number PAIN1876A and lot number 23KLA330 on the kit label.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0514-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0514-2025 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.
