Angiodynamics Inc. (Navilyst Medical Inc.): Medical Device Recall in 2017 - (Recall #: Z-1853-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

NAMIC Fluid Delivery Set - 72" (183cm) UPN H965913000051, Catalog 91300005

Product Classification:

Class II

Date Initiated: January 13, 2017

Date Posted: April 26, 2017

Recall Number: Z-1853-2017

Event ID: 76347

Reason for Recall:

The product has the potential to be non-sterile as it was not packaged in accordance to specification.

Status: Terminated

Product Quantity: 8 boxes/25 units

Code Information:

Lot Number: 5122528

Distribution Pattern:

CA, KY, MD, OR, VA, TX

Voluntary or Mandated:

Voluntary: Firm initiated