Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheter Recalled by Arrow International Inc Due to Arrow is recalling the Arrowgard Blue Plus Antimicrobial...
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
Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheter, catalogue number AK-45854-CDC.
Quantity: 170
Why Was This Recalled?
Arrow is recalling the Arrowgard Blue Plus Antimicrobial Multi-lumen Central Venous Catheter due to a labeling inconsistency. One portion of the lidstock states that the kit contains 8.5FR x 16CM catheter, while the rest of the lidstock correctly identifies the catheter as 8.5FR x 20CM
Where Was This Sold?
This product was distributed to 12 states: AZ, DE, GA, IL, IA, LA, MI, NC, OR, PA, VA, WV
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