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

Recall Z-2591-2023 — Arrow ErgoPack, Pressure Injectable Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percutaneous, implanted, long-term intravascular catheter

U.S. FDA — Device Enforcement · United States · 2023-08-10 · 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-2591-2023
Date of alert
2023-08-10
Country / jurisdiction
United States
Risk level
Class II
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.

Related

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.