Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Recalled by Arrow International Inc Due to Products may contain the incorrect banner card within...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Arrow International Inc directly.
Affected Products
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.
Quantity: 231 units
Why Was This Recalled?
Products may contain the incorrect banner card within the kit
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Arrow International Inc
Arrow International Inc has 431 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report