Medline recalls custom nasal procedure kits (REF DYNJ67789A) due to potential endotoxin contamination in non-sterile surgical components. Affected kits may pose infection risks if used without proper sterilization.
Custom convenience kits are being recall because the contain non-sterile Codman Surgical Patties & Surgical Strips, which have the potential for endotoxin contamination.
Medline is recalling custom nasal procedure kits labeled as NASAL PACK with reference number DYNJ67789A because they contain non-sterile surgical components that could lead to endotoxin contamination. Using these kits without proper sterilization might increase infection risk.
The kits contain non-sterile Codman Surgical Patties and Surgical Strips that could introduce endotoxins, which are bacterial components that may cause infections if not properly sterilized. Endotoxins can lead to infections, especially in medical procedures where sterility is critical.
Healthcare professionals using Medline custom nasal procedure kits with reference number DYNJ67789A are most at risk if they use the kits without proper sterilization.
Check for kits labeled 'NASAL PACK' with reference number DYNJ67789A. Look for lot numbers 21GBW066, 21JBK474, 21KBS434, or 21KBX401 on the packaging.
Look for the reference number DYNJ67789A and lot numbers 21GBW066, 21JBK474, 21KBS434, or 21KBX401 on the kit packaging.
The recall is due to potential endotoxin contamination in non-sterile Codman Surgical Patties and Surgical Strips inside the kits.
Using these kits without proper sterilization could lead to infections due to endotoxins, which are bacterial components.
Check for kits labeled 'NASAL PACK' with reference number DYNJ67789A and lot numbers 21GBW066, 21JBK474, 21KBS434, or 21KBX401.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0781-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0781-2025 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.
