Medline recalls procedure kits with potential catheter insertion issues if connectors aren't fully open. Affected kits include specific models 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 certain procedure kits that may not allow catheters to be inserted correctly if the connector isn't fully open. This could lead to improper catheter placement during medical procedures.
The connectors in these procedure kits may not stay fully open, which can prevent catheters from being inserted as intended. This could result in improper catheter placement during medical procedures.
Healthcare professionals using Medline procedure kits with the specific model numbers and lot numbers listed in the recall. Patients receiving procedures using these kits are at risk of improper catheter placement.
Check for the following model numbers and lot numbers: CONT EPI 20G W/HUSTEAD (REF PAIN1069B), CSE TRAY (REF PAIN1941), and other kits with specific reference codes and lot numbers listed in the recall notice.
Identify the product model and lot number from the kit's label to confirm if it's affected.
Reach out to Medline for assistance with the recall process if you have the affected kit.
The affected models include CONT EPI 20G W/HUSTEAD (REF PAIN1069B), CSE TRAY (REF PAIN1941), and other kits with specific reference codes and lot numbers listed in the recall notice.
Check the product label for the model numbers and lot numbers listed in the recall notice, such as REF PAIN1069B or lot numbers like 22GLA433.
Contact Medline directly to determine the next steps for your specific kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0513-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0513-2025 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.
