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

Recall Z-0563-2022 — 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"

U.S. FDA — Device Enforcement · United States · 2022-01-24 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0563-2022
Date of alert
2022-01-24
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Argon Medical Devices, Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
11377499
Reported risk: Guidewire included with two lots of Arterial Line Kits would not fit through the needle of the same kit. This could potentially lead to a slight delay in the procedure and minor blood loss.
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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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.