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

Recall Z-2556-2019 — Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.

U.S. FDA — Device Enforcement · United States · 2019-08-06 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2556-2019
Date of alert: 2019-08-06
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Arrow International Inc
Product category: device
Product type: Devices

Reported risk: Products may contain the incorrect banner card within the kit

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.

Recall Z-2556-2019 — Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.

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