Medline recalls several medical procedure kits with potential catheter issues including surface finish irregularities and premature connector detachment. Affected kits have specific model numbers 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 medical procedure kits that may have catheter surface finish irregularities and premature connector detachment. These issues could lead to improper medical procedures if the kits are used.
The recalled kits have catheter surface finish irregularities and instances where the catheter connector may detach prematurely from the catheter funnel. This could lead to improper medical procedures if the kits are used.
Healthcare professionals and medical facilities using the recalled Medline procedure kits are most at risk. The affected kits are used in medical procedures.
Check for the following kit labels: BNT CV PACK (SKU DYNJ912271), CV PACK PART 1 (SKU DYNJ31204D), KIT PERIPHERAL VASCULAR MMC (SKU DYNJ905368D), KIT PERIVASCULAR MMC (SKU DYNJ905368B), and VP SHUNT PACK (SKU DYNJ46530I).
Look for the specific model numbers and lot numbers listed in the recall notice to confirm if your kit is affected.
The affected kits include BNT CV PACK (SKU DYNJ912271), CV PACK PART 1 (SKU DYNJ31204D), KIT PERIPHERAL VASCULAR MMC (SKU DYNJ905368D), KIT PERIVASCULAR MMC (SKU DYNJ905368B), and VP SHUNT PACK (SKU DYNJ46530I).
The kits may have catheter surface finish irregularities and instances where the catheter connector may detach prematurely from the catheter funnel, which could lead to improper medical procedures.
The recall indicates potential issues but does not require immediate discontinuation. Check the specific model numbers and lot numbers to confirm if your kit is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2488-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2488-2026 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.
