Medline recalls specific medical procedure kits with catheter surface finish irregularities and connector detachment risks. Affected kits include CAROTID NEURO PACK and VP SHUNT CDS models with certain 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 specific medical procedure kits that have issues with catheter surface finish and connectors detaching prematurely. These problems could lead to medical complications during procedures if the kits are used.
The catheters in these kits have irregular surface finishes and connectors that may detach from the catheter funnel during use. This could cause medical complications if the kits are used in procedures where precise connections are critical.
Healthcare professionals using the recalled Medline Medical Procedure Kits for procedures like carotid neurology or ventriculoperitoneal shunt surgeries. Patients undergoing these procedures are at risk if the kits are used without the recall fix.
Check for Medline Medical Procedure Kits labeled as CAROTID NEURO PACK (SKU DYNJ44926G) or VP SHUNT CDS (SKUs CDS983800J and CDS983800K). Look for specific lot numbers listed in the recall notice.
Look for the product name and SKU on the kit packaging to confirm if it matches the recalled models.
Reach out to Medline Industries, LP directly for assistance with the recall process.
Medline identified that some samples of these kits did not meet performance specifications, including catheter surface finish issues and connector detachment problems.
CAROTID NEURO PACK (SKU DYNJ44926G) and VP SHUNT CDS (SKUs CDS983800J and CDS983800K) with specific lot numbers listed in the recall notice.
Check the kit label for the product name and SKU, then compare the 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-2500-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2500-2026 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.
