Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051 Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to The product has the potential to be non-sterile...
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 Angiodynamics Inc. (Navilyst Medical Inc.) directly.
Affected Products
NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005
Quantity: 8 boxes/25 units
Why Was This Recalled?
The product has the potential to be non-sterile as it was not packaged in accordance to specification.
Where Was This Sold?
This product was distributed to 6 states: CA, KY, MD, OR, TX, VA
About Angiodynamics Inc. (Navilyst Medical Inc.)
Angiodynamics Inc. (Navilyst Medical Inc.) has 78 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report