Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT Recalled by AngioDynamics Inc. Due to Procedure Products initiated the recall due to the...
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. directly.
Affected Products
NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT, REF Catalog No. 601319810, UPN Product No. H7496013198101 Product Usage - This needle is intended to be placed over the guidewire to enlarge the opening in the vessel, and is then removed before sliding the catheter over the guidewire.
Quantity: 45 kits
Why Was This Recalled?
Procedure Products initiated the recall due to the inner lumen of the needles not meeting the intended specification. Specifically, at least a portion of the affected lot is unable to accept a 0.038" guidewire as intended. In some cases the inner lumen was found to be 0.036".
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About AngioDynamics Inc.
AngioDynamics Inc. has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report