Medline recalls specific medical procedure kits due to irregular catheter surface finish and connector detachment risks. Affected kits include RETINA LAC/USC and TONSIL PACK 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 irregularities in catheter surface finish and may detach prematurely. This could lead to improper use during medical procedures if the kits are used without addressing these issues.
The recalled kits have catheters that may have surface finish irregularities and connectors that can detach from the catheter funnel. This could lead to improper use during medical procedures if the kits are used without addressing these issues.
Healthcare professionals and medical facilities that use the recalled Medline procedure kits are most at risk. The recall affects specific kits used in eye and throat procedures.
Check for kits labeled as RETINA LAC/USC CDS with SKUs CDS983775I-J and TONSIL PACK with SKU DYNJ84480. Look for specific lot numbers listed in the recall notice.
Review the product label for the specific SKU and lot number listed in the recall notice.
The recall indicates potential issues with catheter surface finish and connector detachment, so they should not be used until the recall is addressed.
Check for kits labeled as RETINA LAC/USC CDS with SKUs CDS983775I-J or TONSIL PACK with SKU DYNJ84480, and verify the lot number against the list provided in the recall.
The recall does not specify a remedy, so contact Medline directly for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2507-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2507-2026 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.
