Medline recalls custom cervical procedure kits due to potential endotoxin contamination from non-sterile surgical materials. Affected kits include specific model numbers and lot ranges. Consumers should contact Medline for details.
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 for cervical spine surgeries because they contain non-sterile surgical materials that could lead to endotoxin contamination. This poses a risk of infection or other complications for patients during medical procedures.
The kits contain non-sterile Codman Surgical Patties and Surgical Strips that can introduce endotoxins, which are bacterial components that may cause infections or adverse reactions when used in medical procedures.
Healthcare providers using Medline's custom cervical procedure kits for spine surgeries are most at risk. Patients receiving these kits during procedures may face infection risks if the materials are contaminated.
Check for kit labels with model numbers: CERVICAL PACK-LF (REF DYNJ0867145G), CERVICAL SPINE PACK HUM-LF (REF DYNJ35184F), or ANTERIOR CERVICAL-CORPECTOMY (REF DYNJ904827). Also look for lot numbers like 19BDA435 or 19CBC965.
Reach out to Medline directly for specific instructions on how to return or replace the recalled kits.
No, the kits contain non-sterile materials that could lead to endotoxin contamination, posing a risk of infection during medical procedures.
Contact Medline to get instructions for returning or replacing the recalled kits.
Kits labeled as CERVICAL PACK-LF (REF DYNJ0867145G), CERVICAL SPINE PACK HUM-LF (REF DYNJ35184F), or ANTERIOR CERVICAL-CORPECTOMY (REF DYNJ904827) with specific lot numbers.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0793-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0793-2025 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.
