Medline recalls custom medical procedure kits (CRANI, CRANIOFACIAL, CRANIOTOMY, etc.) due to potential endotoxin contamination in non-sterile Codman Surgical Patties & Surgical Strips. Affected kits have specific REF numbers and lot numbers listed in the recall.
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 medical procedure kits labeled with specific REF numbers (e.g., CRANI, CRANIOFACIAL) because they contain non-sterile Codman Surgical Patties & Surgical Strips that may have endotoxin contamination. This could pose a risk of infection or other complications during medical procedures.
The kits contain non-sterile Codman Surgical Patties & Surgical Strips that may have endotoxin contamination. Endotoxins are bacterial components that can cause infections or adverse reactions if introduced into the body during medical procedures.
Healthcare professionals and medical facilities that use these kits are most at risk. Patients using these kits during surgery could be exposed to endotoxins.
Check for kits labeled with REF numbers like CRANI (CDS780089V), CRANIOFACIAL (CDS780102K), CRANIOTOMY (CDS780105K), or other specific model numbers listed in the recall. Also look for associated lot numbers and UDI/DI codes.
Identify if your kit matches the REF numbers and lot numbers listed in the recall (e.g., CRANI, CRANIOFACIAL, CRANIOTOMY with specific REF codes).
Reach out to Medline for guidance on next steps if your kit is affected.
The kits contain non-sterile Codman Surgical Patties & Surgical Strips that may have endotoxin contamination, which could lead to infection or adverse reactions during medical procedures.
Check for kits labeled with REF numbers like CRANI (CDS780089V), CRANIOFACIAL (CDS780102K), CRANIOTOMY (CDS780105K), or other specific model numbers listed in the recall. Also look for associated lot numbers and UDI/DI codes.
The recall does not specify a discard action; contact Medline for guidance if your kit is affected.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0794-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0794-2025 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.
