Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Radial Artery Catheterization Set Recalled by Arrow International Inc Due to Needle supplier indicated the presence of loose polypropylene...
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
Radial Artery Catheterization Set, 1) NA-04550-1A & 2) NA-04550-X1A, device permits access to the peripheral arterial circulation or to other small vessels.
Why Was This Recalled?
Needle supplier indicated the presence of loose polypropylene foreign matter above release specification.
Where Was This Sold?
...
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