Medical device recalls Moderate risk

Medline Industries, LP recalls Medline Convenience Kits: 1) WMC I D PACK-LF, Model Number: DYNJ50806L

Recall date
January 7, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1403-2026
FDA classification
Class II
Brand / firm
Medline Industries, LP
Sold / distributed
Worldwide distribution - US Nationwide.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Medline Convenience Kits: 1) WMC I D PACK-LF, Model Number: DYNJ50806L

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