Medline recalls 14 medical procedure kits with irregular catheter surfaces and connector detachment risks. Affected kits include BASIC HEART PACK and CARDIAC SURGERY models with specific SKUs and lot numbers.
During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.
Medline is recalling 14 different medical procedure kits due to issues with catheter surfaces and connectors. These problems could lead to improper use during medical procedures if the catheters detach or have uneven surfaces.
The recalled kits have catheters with irregular surface finishes, connectors that can detach prematurely from the catheter funnel, and outer diameters that don't meet specifications. These issues could lead to improper use during medical procedures.
Healthcare professionals using these kits for medical procedures are most at risk. The recall affects specific models and lot numbers of Medline medical procedure kits.
Check for Medline kits labeled as BASIC HEART PACK (SKU DYNJ67331B), CARDIAC SURGERY (SKU DYNJ911589A), or other listed models with specific lot numbers and UDI/DI codes.
Look for the product name, SKU, and lot number on the kit label to confirm if it's affected.
The recall indicates potential issues with catheter surface finish and connector detachment, so they should not be used until replaced with confirmed safe models.
Check the product name, SKU, and lot number on the kit label against the list of affected models and lot numbers provided in the recall notice.
The recall does not specify a remedy, so contact Medline directly for guidance on safe alternatives or disposal.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2486-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2486-2026 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.
