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

Recall Z-3299-2024 — Arrow Arterial Kits and Trays as follows: (1) Arrow Arterial Access Tray with 0.025" Spring-Wire Guide (Catheter Not Included), REF ASK-04001-BW1; (2) Arrow Arterial Access Tray with 0.021" Spring-Wire Guide (Catheter Not Included), REF ASK-04001-CK; (3) Arrow Arterial Access Kit, .025 in

U.S. FDA — Device Enforcement · United States · 2024-07-26 · 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-3299-2024
Date of alert: 2024-07-26
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: ARROW INTERNATIONAL Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10801902117585

Reported risk: Reports have been received regarding open seals on the packaging.

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