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

Recall Z-0004-2024 — Arrow ErgoPack Pressure Injectable Arrowg+ard Blue Advance Three-Lumen PICC pre-loaded with Arrow VPS TipTracker Stylet, REF CDC-45563-TTS; catheter, intravascular, therapeutic, long-term greater than 30 days

U.S. FDA — Device Enforcement · United States · 2023-08-10 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0004-2024
Date of alert
2023-08-10
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
ARROW INTERNATIONAL Inc.
Product category
device
Product type
Devices
Reported risk: This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
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.