Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arrow International Recalled by Arrow International Inc Due to Arrow is recalling the product due to a...
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 International, Inc. Two-Lumen CVC Kit with Blue Flex Tip Catheter. The multiple lumen catheter permits venous access to the central circulation of patients.
Quantity: 156
Why Was This Recalled?
Arrow is recalling the product due to a labeling inconsistency. One portion of the lidstock states the kit contains a 3-Lumen catheter while the rest of the lidstock correctly identifies the catheter as 2-Lumen.
Where Was This Sold?
This product was distributed to 10 states: AL, AZ, CT, IL, KS, NJ, NC, PA, RI, VA
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