Medline recalls specific medical convenience kits due to potential endotoxin levels in Neurosponges. Affected kits include SINUS PACK-LF and ENT PACK models with certain SKUs and lot numbers.
Specific item(s) and lot(s) of Medline convenience kits containing Pilling Wecksorb Neurosponges and Neurosponge Strips are being recalled due to potential out-of-specification levels of endotoxin of the neurosponges.
Medline is recalling medical convenience kits that contain Neurosponges with potential endotoxin levels outside specifications. This could pose a risk to users, especially those with compromised immune systems.
The neurosponges in these kits may have endotoxin levels that are outside the specified safety range. Endotoxins are bacterial components that can cause adverse reactions in sensitive individuals.
Healthcare professionals and medical facilities using Medline convenience kits are most at risk. Individuals with weakened immune systems may be affected by the endotoxin levels.
Check for the following SKUs: DYNJ0966146F, DYNJ40154D, DYNJ40154F, DYNJ44480D, DYNJ58928A, DYNJ83296, DYNJ89006, DYNJ900537D, DYNJ900537F, DYNJ903679F, DYNJ903679G, DYNJ903679I, DYNJ903679J, DYNJ903679K. Lot numbers 23HBC070 through 25KBT345 are affected.
Identify the SKU and lot number on the kit to confirm if it is affected.
The neurosponges in these kits may have endotoxin levels outside the specified safety range.
SINUS PACK-LF (SKU DYNJ0966146F) and ENT PACK kits with SKUs DYNJ40154D, DYNJ40154F, DYNJ44480D, DYNJ58928A, DYNJ83296, DYNJ89006, DYNJ900537D, DYNJ900537F, DYNJ903679F, DYNJ903679G, DYNJ903679I, DYNJ903679J, DYNJ903679K.
Check the SKU and lot number on the kit. Affected kits have specific SKUs and 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-2994-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2994-2026 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.
