Medline recalls convenience kits with Swan-Ganz catheters that may leak or break, risking infection and blood loss. Affected kits have specific model numbers and lot codes.
Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to instances of leakage, lumen damage, and breakage, and may lead to infection, medication loss, and/or blood loss.
Medline is recalling convenience kits that include Swan-Ganz catheters with a known risk of leaking or breaking. This could lead to infections, medication loss, or blood loss if the catheter fails.
The catheters have a faulty blue proximal injectate lumen hub that can leak or break. This failure may cause infections, medication loss, or blood loss during medical procedures.
Healthcare professionals using Medline convenience kits with the recalled Swan-Ganz catheters are most at risk. Patients receiving care with these kits may also be affected.
Check for model numbers DYNJ909090B or CDS982523M on the kit. Look for lot codes like 24EBL051, 24GBG271, or 24ALA227.
Identify the model number on the kit (DYNJ909090B or CDS982523M) and lot codes.
Reach out to Medline for assistance with the recall process.
BD has received complaints of leaks and breakage in the blue proximal injectate lumen hub of these catheters, which can lead to infections, medication loss, or blood loss.
Check for model numbers DYNJ909090B or CDS982523M and lot codes like 24EBL051, 24GBG271, or 24ALA227.
Contact Medline directly for guidance on the recall process.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2611-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2611-2026 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.
