Medline Industries, LP recalls Medline medical convenience kits

Recalling company

Medline Industries, LP

Product

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.

Reason

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

Classification

Class I – a reasonable probability that use will cause serious adverse health consequences or death

Recall date

Mar 24, 2026

Reported

May 20, 2026

Distribution

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

Status

Ongoing

Quantity

508 kits

Lot / codes

Medline Kit Number/SKU DYNJ23532C: UDI/DI each 10193489460872, UDI/DI case 40193489460873, Lot Number: 25DMA809; Medline Kit Number/SKU DYNJ65185: UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number: 23GBA252; Medline Kit Number/SKU DYNJ65185: UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number: 23HBI873; Medline Kit Number/SKU DYNJ65185: UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number: 23IBR043; Medline Kit Number/SKU DYNJ65185: UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number: 23KBF277; Medline Kit Number/SKU DYNJ65185: UDI/DI each 10193489253146, UDI/DI case 40193489253147, Lot Number: 24ABQ959; Medline Kit Number/SKU VASC1057: UDI/DI each 10889942431922, UDI/DI case 40889942431923, Lot Number: 25KMF194.

Company location

Northfield, IL

Recall type

Voluntary: Firm initiated

Recall number

Z-2143-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2143-2026 in the FDA Enforcement Report. Also see FDA recall press releases.