Medline recalls convenience kits with Swan-Ganz catheters (DYNJ8407) due to potential leaks and breakage from catheter hub failures, risking infection and blood loss.
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 specific model number. These kits may have catheters that leak or break, which could lead to infections or blood loss if used in medical settings.
The catheters' blue proximal injectate lumen hub can fail, causing leaks, lumen damage, or breakage. This may result in infections, medication loss, or blood loss during medical procedures.
Healthcare professionals using Medline convenience kits with Swan-Ganz catheters (model DYNJ8407) are most at risk. Patients receiving these catheters could face infections or blood loss if the catheters leak or break.
Check for Medline convenience kits labeled with model DYNJ8407. The kits may also have a UDI-DI number 10198459704543 and lot number 26DBB599.
Look for the model number DYNJ8407 on the kit label or packaging.
BD has received complaints of leaks and breakage in the Swan-Ganz catheters, which can cause infections, medication loss, or blood loss.
The recall record does not specify a remedy, so contact Medline directly for guidance.
Check for the model number DYNJ8407 and UDI-DI number 10198459704543 on the kit label or packaging.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2608-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2608-2026 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.
