Class II — Potential Health Hazard

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...

Date: January 13, 2017
Company: Angiodynamics Inc. (Navilyst Medical Inc.)
Status: Terminated
Source: FDA (Device)

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

Affected (6 states)Not affected

About Angiodynamics Inc. (Navilyst Medical Inc.)

Angiodynamics Inc. (Navilyst Medical Inc.) has 78 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report