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

Recall Z-1916-2026 — MAC" Two-Lumen Central Venous Access Kit for use with 7.5 - 8 Fr. Catheters REF ASK-11142-LC2 UDI code: (01)10801902206807(17)270531(11)251211(10)33F25M0670 The MAC Multi-Lumen Central Venous Access Device permits short-term (<30 days) venous access and catheter introduction to the central circ

U.S. FDA — Device Enforcement · United States · 2026-03-11 · Class II

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1916-2026
Date of alert: 2026-03-11
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: ARROW INTERNATIONAL, LLC
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10801902206807

Reported risk: Due to receiving a notice from a supplier that the liquid adhesive was incorrectly manufactured

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.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Related