FDAJanuary 7, 2026device

Medline Convenience Kits: 1) KIT GENERAL CLOSURE, Model Number: DYKMBNDL200A

Official recall recorded by the U.S. Food & Drug Administration.

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.

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lpmedlinemedline industries

UPCs

1019532724059240195327240593

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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