Medline Triple Lumen Insertion Kit Recall
Medline Convenience Kits: 1) KIT TRIPLE LUMEN INSERTION, Model Number: DYNDM1031A
Updated January 7, 2026
Medline is recalling Triple Lumen Insertion Kits due to sterilization equipment calibration issues that may have compromised the sterility of the devices. Use of non-sterile medical equipment can lead to serious infection.
Is the Medline Industries, LP recalled? Yes. This product was recalled by FDA on January 7, 2026. Details below.
What is recalled
Medline Convenience Kits: Triple Lumen Insertion, Model Number DYNDM1031A.
Am I affected
You're affected if you have a Medline Triple Lumen Insertion Kit with model number DYNDM1031A.
What to do right now
Stop using this kit immediately. Contact Medline Industries, LP for return instructions or a replacement. Do not use any affected kits for patient care.
The hazard
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.
Brands affected
- Source
- FDA
- Category
- Medical Devices
- Recall ID
- fda-Z-1407-2026
- Classification
- Class II
- Recalled
- January 7, 2026
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