Medline UDI/DI Case and Lot Numbers for various products including Medline Kit Numbers/SKUs. Find UDI/DI each and case numbers with corresponding lot numbers.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
This document contains a list of UDI/DI case and lot numbers for Medline products. Each entry includes a Medline Kit Number/SKU, UDI/DI each number, UDI/DI case number, and Lot Number. The data spans multiple SKUs and lot numbers with detailed tracking information.
The data is publicly available and does not contain sensitive information that could be misused. It is a standard tracking information for medical devices.
Medical device manufacturers, healthcare facilities, regulatory bodies
Check for any unusual patterns or anomalies in the UDI/DI numbers that might indicate tampering or fraud. Ensure that the lot numbers match the expected production dates and locations.
Verify the UDI/DI numbers against the manufacturer's official database to ensure they are valid and match the product specifications.
Cross-check the lot numbers with the production dates and locations to confirm they align with the expected manufacturing timeline.
Ensure that the UDI/DI case numbers correspond to the physical packaging and that the lot numbers are consistent across all units.
UDI/DI (Unique Device Identification/Device Identifier) is a unique code assigned to medical devices to ensure traceability throughout the supply chain.
You can verify the authenticity of a UDI/DI number by checking it against the manufacturer's official database or using the FDA's UDI database for US products.
The lot number is a unique identifier for a batch of products produced during a specific manufacturing run. It helps in tracking and recalling products if necessary.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2145-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2145-2026 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.
