Medline Industries, LP offers a wide range of medical products including surgical instruments, PPE, and more. Explore our catalog for quality healthcare solutions.
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
Medline Industries, LP is a leading manufacturer of medical products with a focus on surgical instruments, personal protective equipment (PPE), and healthcare solutions. Their products are designed to meet the highest standards of quality and safety for healthcare professionals.
Low risk due to standard medical product usage and compliance with regulatory standards.
Healthcare professionals, medical facilities, and patients
Check for proper labeling, UDI-DI codes, and lot numbers to ensure product authenticity and traceability.
The UDI-DI code is a unique identifier for the product. For example, in the data provided, the UDI-DI for DYNJ64936B is 10195327223205.
Lot numbers are used to track products through the supply chain. For example, the lot number for DYNJ64936B is 23DBP201.
The UDI-DI code is a 13-digit code that uniquely identifies a specific product. It helps in tracking and managing medical devices throughout their lifecycle.
Compare the UDI-DI code and lot number with the information provided by the manufacturer. Authentic products will have matching codes and lot numbers.
A UDI-DI code is a unique identifier for medical devices. It helps in tracking and managing medical devices throughout their lifecycle.
Lot numbers are used to trace products back to the manufacturer and specific production batch. They help in recalls and quality control.
The UDI-DI code ensures that medical devices can be uniquely identified and tracked, which is critical for patient safety and regulatory compliance.
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-1835-2026 — Medline Industries, LP Medline Industries, LP Hello, I own a Medline Industries, LP that is covered by recall Z-1835-2026 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.
