Medline recalls specific medical procedure kits due to irregular catheter surface finish and connector detachment risks. Affected kits include CRANI and other surgical kits with listed 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 certain medical procedure kits that have irregular catheter surface finishes and may detach connectors prematurely. This could lead to improper medical procedures if used.
The recalled kits have catheters with irregular surface finishes and connectors that may detach from the catheter funnel. This could cause improper medical procedures if the kits are used without these issues being corrected.
Healthcare professionals and medical facilities using the recalled Medline procedure kits are most at risk. The issue affects specific kits with listed SKUs and lot numbers.
Check for Medline kits labeled CRANI with SKUs DYNJ908097 through DYNJ908097D, DYNJ912029, DYNJ55637B, DYNJ43930A, DYNJ67767, DYNJ61136F, or DYNJV0172Q. Look for the specific lot numbers listed in the recall notice.
Verify the kit's SKU and lot number against the list provided in the recall notice to confirm if it is affected.
The recall indicates potential issues with catheter surface finish and connector detachment, so they should not be used until confirmed safe.
Check the kit's SKU and lot number against the list of affected items in the recall notice.
The recall does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2508-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2508-2026 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.
