Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Recalled by Arrow International Inc Due to These finished good kits may contain the incorrect...
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
Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product Code: ASK 42703 PUHC; Exp. Dates Feb 2018 - Nov 2018
Quantity: 5,926 total
Why Was This Recalled?
These finished good kits may contain the incorrect Springwire Guide (SWG).
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