Medline recalls medical procedure kits with irregular catheter surfaces and connector detachment risks. Affected kits have specific model numbers and lot dates.
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 medical procedure kits that have irregular catheter surfaces and may detach prematurely. This could lead to improper medical procedures if used.
The catheters in these kits have irregular surfaces and may detach from the funnel. This could cause improper medical procedures if the kit is used without the connector staying attached.
Healthcare professionals using Medline medical procedure kits with the specified model numbers and lot dates are most at risk. Patients receiving procedures using these kits may also be affected.
Check for kits labeled 'D AND C PACK' with Medline SKU DYNJ53973C or 'PK CUST CV A&B' with SKU DYNJ60583C. Look for lot numbers 21KME435, 21JMC247, 21JMB678, or 21IMH919 for the first SKU, and lot numbers 24CBO389 or 24ABR872 for the second SKU.
Look for the specific model numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
The recall states that representative samples did not meet performance specifications, but the kits may still be safe for use if used properly. However, Medline recommends checking if your kit is affected.
The recall does not specify a remedy, so you should check with Medline directly for further instructions.
Check for the specific model numbers and lot numbers listed in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2504-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2504-2026 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.
