Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
XCELA Recalled by Angiodynamics Inc. (Navilyst Medical Inc.) Due to Snap lock connectors provided within implantable port kits...
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
XCELA, 8F SINGLE PLASTIC PORT FILLED, VALVED, UPN H965440400, Cat. No. 44-040 - Product Usage: Long-term access to the central venous system for administration of fluids including but not limited to hydration fluids, chemotherapy, analgesics, nutritional therapy and blood products. The device is also indicated for blood specimen withdrawal.
Quantity: 582
Why Was This Recalled?
Snap lock connectors provided within implantable port kits may not meet dimensional specifications, and the catheter cannot be inserted into the snap lock connector prior to connection to the port chamber, resulting in a delay to the implantation procedure.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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