Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to The povidone iodine prep pads included in certain...
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 Kit; Model: AK-04018
Quantity: 930
Why Was This Recalled?
The povidone iodine prep pads included in certain kits and trays do not meet the requirements for a 36-month shelf life and should be labeled with a 24-month shelf life.
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