Medline Industries, LP - 2001S, 2002, 2002S
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 - 2001S, 2002, 2002S
No specific danger
All
Check for proper labeling and compliance with safety standards
Verify the product's UDI-DI and Lot Number against the manufacturer's records to ensure they match the expected specifications.
Ensure that the product is within the valid usage period and has not expired.
Check for any recalls or warnings related to the specific product model and lot number from the manufacturer's website or regulatory databases.
The UDI-DI for Medline Industries, LP products is typically a unique identifier that includes the product type and model. The Lot Number is a specific batch number assigned to each production run. For example, UDI-DI: 10080196304660(each), 40080196304661(case), Lot Number: 72524010088.
Check the product's UDI-DI and Lot Number against the manufacturer's records to ensure they match the expected specifications. Also, ensure the product is within the valid usage period and has not expired.
Contact Medline Industries, LP directly or report the issue to the relevant regulatory authority to ensure the product's safety.
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-2129-2026 — Medline Industries, LP Medline Industries, LP Hello, I own a Medline Industries, LP that is covered by recall Z-2129-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
