Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arrow ErgoPack Recalled by ARROW INTERNATIONAL Inc. Due to This recall has been initiated due to reports...
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 ErgoPack, Pressure Injectable Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percutaneous, implanted, long-term intravascular catheter
Quantity: 177 units
Why Was This Recalled?
This recall has been initiated due to reports that the product code and product name were incorrectly listed on the lidstock of affected kits.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ARROW INTERNATIONAL Inc.
ARROW INTERNATIONAL Inc. has 47 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report