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

ARROW RADIAL ARTERY CATHETERIZATION KIT REF ASK-04220-UCL1 UDI code: (01)10801902159127(17)270331(11)251203(10)33F25J0352 REF ASK-04020-EUH2 UDI code: (01)10801902213379(17)270731(11)251218(10)33F25J0869 REF ASK-04020-FMC UDI code: (01)10801902212099(17)270731(11)251218(10)33F25J0870 R — recall Z-1911-2026

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

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1911-2026
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): 10801902159127

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

Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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.

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