Windstone Medical Packaging recalls specific ENT medical kits due to potential endotoxin level variations in Ritmed Neurological Sponges. Affected kits include ENT Packs with pack numbers AMS12206, AMS15517, and AMS15863A.
The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.
Windstone Medical Packaging is recalling ENT medical convenience kits that contain Ritmed Neurological Sponges with potential endotoxin level variations. This could affect the safety of the products if used in medical procedures.
The recalled kits contain Ritmed Neurological Sponges that may have unexpected variations in endotoxin levels. Endotoxins are bacterial components that can cause infections or adverse reactions if the levels are inconsistent during medical procedures.
Medical professionals using the recalled ENT kits are most at risk. Patients receiving procedures with these kits may be affected if the endotoxin levels are inconsistent.
Check for ENT packs with pack numbers AMS12206, AMS15517, or AMS15863A. The kits were sold with specific lot numbers listed in the recall notice.
Identify the pack number and lot numbers listed in the recall notice to confirm if your kit is affected.
The kits contain Ritmed Neurological Sponges that may have unexpected variations in endotoxin levels, which could cause infections or adverse reactions during medical procedures.
ENT packs with pack numbers AMS12206, AMS15517, and AMS15863A, each with specific lot numbers listed in the recall notice.
The recall is for potential endotoxin variability, which is a low-risk hazard. There is no immediate stop-use instruction; check the product details to confirm if your kit is affected.
We’ve drafted a message you can send Windstone Medical Packaging to request your refund or repair — edit it as you like.
Subject: Recall Z-2800-2026 — Windstone Medical Packaging Windstone Medical Packaging Hello, I own a Windstone Medical Packaging that is covered by recall Z-2800-2026 from Windstone Medical Packaging. 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.
