Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2143-2026 — 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.

U.S. FDA — Device Enforcement · United States · 2026-03-24 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2143-2026
Date of alert
2026-03-24
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Medline Industries, LP
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10193489460872
Reported risk: Medline has identified the presence of particulate within the fluid path of the Manifolds.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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