Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Multi-Lumen Central Venous Catheterization Kit Recalled by Arrow International Inc Due to Arrow International, Inc. has initiated a voluntary recall...
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
Multi-Lumen Central Venous Catheterization Kit
Quantity: 65
Why Was This Recalled?
Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date.
Where Was This Sold?
This product was distributed to 10 states: CA, IN, KY, LA, MD, NV, NY, NC, OH, PA
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