Medline recalls specific tonsil pack catheter kits due to irregular catheter surfaces and connector detachment risks. Affected kits have unique 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 tonsil pack catheter kits because some have faulty catheters that may detach or have uneven surfaces. This could lead to improper use during medical procedures.
The catheters may have irregular surfaces that could cause issues during medical procedures. In some cases, the connector might detach from the catheter funnel, potentially leading to improper use.
Healthcare professionals using Medline's TONSIL PACK CATH kits with specific SKUs and lot numbers are most at risk. Patients using these kits may also be affected if the catheter malfunctions.
Check for Medline Kit Number/SKU DYNJ65199A on the kit. Look for lot numbers 23HMI132, 23HMA956, 23GMA525, 23DMF610, 23AMH680, or 22CBF155.
Verify the Medline Kit Number/SKU DYNJ65199A and lot numbers listed in the recall notice.
Medline identified that some kits have irregular catheter surfaces and connectors that may detach prematurely.
The recall notice does not specify a remedy, so check the kit details to confirm if it's affected.
The recall mentions potential issues like catheter detachment and surface irregularities, but no specific injury risks are stated.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2494-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2494-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
