Medline Industries, LP recalls Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SK…

Recall date

March 24, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2143-2026

FDA classification

Class I

Brand / firm

Medline Industries, LP

Sold / distributed

US (nationwide) and AE, AU, CA, JP, KR, NL, SG, SK.

Why it was recalled

Medline has identified the presence of particulate within the fluid path of the Manifolds.

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. ANGIOGRAPHY CATH LAB, Medline Kit Number/SKUDYNJ23532C; 2. CATH LAB PACK, Medline Kit Number/SKUDYNJ65185; 3. ANGIO KIT, Medline Kit Number/SKUVASC1057.