Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arrow Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane Recalled by Arrow International Inc Due to The lidstock label incorrectly displays a MR (Magnetic...
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 Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with Integral .018" (0.46 mm) dia. Spring-Wire Guide Product Code: ASK-04020-PMC The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels.
Quantity: 80 eaches
Why Was This Recalled?
The lidstock label incorrectly displays a MR (Magnetic Resonance ) Conditional symbol (instead of a MR Unsafe symbol) in reference to a component of the kit
Where Was This Sold?
This product was distributed to 1 state: SC
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