Medline recalls specific medical procedure kits due to irregular catheter surface finish and connector detachment risks. Affected kits include CV DRAPING/BASIN models with certain 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 several medical procedure kits that have irregular catheter surface finishes and may cause connectors to detach prematurely. This could lead to improper use during medical procedures.
The recalled kits have catheters with irregular surface finishes and connectors that may detach from the catheter funnel. This could lead to improper use during medical procedures if the connection fails.
Healthcare professionals and medical facilities that use these specific Medline procedure kits are most at risk. The recall affects kits with certain SKUs and lot numbers.
Check for Medline kits labeled as CV DRAPING/BASIN with SKUs DYNJ908483A, DYNJ908483B, DYNJ908483C, DYNJ89414, DYNJ38052G, DYNJ47941F, or DYNJ38054G. Look for specific lot numbers listed in the recall notice.
Review the kit's label for the specific SKU and lot number listed in the recall notice to confirm if it's affected.
The recall indicates potential issues with catheter surface finish and connector detachment, but the remedy is not stated in the record.
The recall record does not specify a remedy, so contact Medline directly for guidance.
Check the kit's label for the specific SKUs 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-2496-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2496-2026 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.
