Medline recalls custom deep brain stimulation procedure kits due to potential endotoxin contamination in non-sterile surgical components. Affected kits may pose infection risks during medical procedures.
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 deep brain stimulation procedure kits because they contain non-sterile surgical components that could be contaminated with endotoxins. This poses a risk of infection during medical procedures if the kits are used without proper sterilization.
The kits contain non-sterile Codman Surgical Patties and Surgical Strips that may have endotoxin contamination. Endotoxins are bacterial components that can cause infections if introduced into the body during medical procedures.
Medical professionals using these specific deep brain stimulation procedure kits are most at risk. Patients receiving procedures with these kits could face infection if the non-sterile components are not properly handled.
Check for kits labeled 'DEEP BRAIN STIMULATION PACK-LF' with specific lot numbers: 19BKB326, 19DKA892, 19JDA775, or 20ADC560. These kits were sold with UDI/DI numbers 10889942825547 (EA) and 40889942825548 (CS).
Look for the label 'DEEP BRAIN STIMULATION PACK-LF' and specific lot numbers: 19BKB326, 19DKA892, 19JDA775, or 20ADC560.
The recall is due to potential endotoxin contamination in non-sterile Codman Surgical Patties and Surgical Strips, which could lead to infection during medical procedures.
The official recall notice does not specify a remedy or action steps beyond checking the label for affected kits.
The recall indicates these kits may contain non-sterile components with endotoxin contamination risk, so they should not be used without proper sterilization.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0791-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0791-2025 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.
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.
