Medline recalls custom medical procedure kits with non-sterile surgical components that may contain endotoxins. Affected kits include specific models and lot numbers; users 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 that contain non-sterile surgical components which could lead to endotoxin contamination. This poses a risk of infection or complications during medical procedures.
The kits include non-sterile Codman Surgical Patties and Surgical Strips that may contain endotoxins. Endotoxins are bacterial components that can cause infections or adverse reactions when introduced into the body during medical procedures.
Medical professionals using the recalled kits are most at risk. Patients undergoing procedures with these kits could face infection or complications.
Check for kits labeled with model numbers DYNJ58648B, DYNJ58648C, DYNJ66447, DYNJ58648D, or DYNJ58648J. Look for specific lot numbers listed in the recall notice.
Reach out to Medline for specific instructions on how to return or replace the affected kits.
The kits contain non-sterile Codman Surgical Patties and Surgical Strips that may have endotoxin contamination, which could lead to infections or complications during medical procedures.
The affected kits include models labeled DYNJ58648B, DYNJ58648C, DYNJ66447, DYNJ58648D, and DYNJ58648J with specific lot numbers.
Check the model numbers and lot numbers listed in the recall notice, which include the specific codes and numbers provided in the product descriptions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0784-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0784-2025 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.
