Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Femoral Arterial Line Catheterization Kit with Sharps Safety Features 510K Recalled by Arrow International Inc Due to Labeling error. Some shipping cartons labeled as ASK-04018-VUH...
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
Femoral Arterial Line Catheterization Kit with Sharps Safety Features 510K 810675, product code DQX, Device Listing D025180 Material ASK-04018-VUH Product Usage: The Arrow arterial catheterization device permits access to the peripheral arterial circulation.
Quantity: 50 units in total
Why Was This Recalled?
Labeling error. Some shipping cartons labeled as ASK-04018-VUH contained ASK-04020-VUH kits; and some shipping cartons labeled as ASK-04020-VUH contained ASK-04018-VUH kits.
Where Was This Sold?
This product was distributed to 2 states: KY, TN
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