Medline Industries, LP is a leading provider of medical supplies, equipment, and products for healthcare facilities and professionals.
During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.
Medline Industries, LP is a well-known manufacturer of medical supplies and equipment. They offer a wide range of products including surgical instruments, diagnostic tools, and patient care items. Their products are used in hospitals, clinics, and other healthcare settings.
The products are designed for medical use and are generally safe when used as intended. However, like all medical devices, they should be handled with care to avoid injury or contamination.
Healthcare professionals, hospitals, clinics, and medical facilities
Check for proper labeling, expiration dates, and compliance with medical standards.
Ensure that the UDI/DI and lot number match the information provided on the product label.
Make sure the product has not expired before use.
Compare the manufacturer name and product details with the information provided on the product label.
Follow the manufacturer's instructions for handling and storage to maintain product integrity.
UDI/DI stands for Unique Device Identification/Device Identifier. It is a unique code assigned to medical devices to track them throughout their lifecycle.
Medline products are designed to meet medical standards and are generally safe when used as intended. Always check for proper labeling, expiration dates, and compliance with medical standards.
Contact Medline customer service or your healthcare facility's supply chain department for assistance. They will guide you through the appropriate steps for returns or replacements.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2025-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2025-2026 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.
