Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Catheter Recalled by Arrow International Inc Due to Notification of component molding abnormality by supplier used...
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
Catheter, Intravascular, Therapeutic, Short-Term Less than 30 days The Arrow CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access.
Quantity: 6,121 units in total
Why Was This Recalled?
Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.
Where Was This Sold?
This product was distributed to 4 states: FL, MD, NC, OH
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