Medline recalls medical convenience kit TRACH TUBE KIT (SKU DYKM2330) due to labeling discrepancy. Affected units have specific UDI/DI and lot numbers. No remedy stated in official notice.
Component labeling discrepancy
Medline is recalling a medical convenience kit labeled as TRACH TUBE K: the kit has a labeling discrepancy that could cause confusion. This recall affects specific units with the UDI/DI 10198459582158 (each) and 40198459582159 (case), lot number 26FLA408. The issue does not pose an immediate safety risk but requires correction to prevent misidentification.
The labeling discrepancy means the kit's name and identifiers don't match the actual product. This could lead to incorrect identification or use of the kit, potentially causing errors in medical procedures. However, the issue does not involve physical harm or immediate safety risks.
Medical professionals and facilities using Medline's TRACH TUBE KIT (SKU DYKM2330) with the specified UDI/DI and lot numbers are affected. Those handling medical equipment without proper labeling may be at higher risk of confusion.
Check for the label 'TRACH TUBE KIT' and the specific UDI/DI numbers: 10198459582158 (each) and 40198459582159 (case), with lot number 26FLA408. The kit is sold under Medline Industries, LP.
Verify the UDI/DI numbers and lot number on the kit to confirm if it is affected.
No, the recall is for labeling discrepancy only. It does not pose an immediate safety risk but could cause confusion in medical use.
The official notice does not state a remedy, so check the label details to confirm if it is affected.
Look for the label 'TRACH TUBE KIT' with UDI/DI numbers 10198459582158 (each) and 40198459582159 (case), and lot number 26FLA408.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2999-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2999-2026 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.
+ 1 more story
