Medline Industries, LP - 236-359
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
Medline Industries, LP - 236-359
No specific danger
All
Check for proper labeling and ensure the product is within the expiration date
Inspect the product for any visible damage, such as cracks, dents, or other physical issues that could affect its functionality or safety.
Ensure the product has not expired and is within the recommended usage period.
Compare the lot numbers and UDI-DI information with the provided data to ensure they match the expected specifications.
The UDI-DI for the product is 10198459475337 (each) and 40198459475338 (case).
The lot number for the product is 25IMH581, 25LMF022, 25LMH340, etc.
Check for any signs of damage or defects, verify the expiration date, and ensure the lot number and UDI-DI information match the expected specifications.
We’ve drafted a message you can send Medline Industries, LP to request your refund or repair — edit it as you like.
Subject: Recall Z-2093-2026 — Medline Industries, LP Medline Industries, LP Hello, I own a Medline Industries, LP that is covered by recall Z-2093-2026 from Medline Industries, LP. 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.
