Angiodynamics, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0132-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Vortex MP Port Titanium Low Profile Implanted Port with 5F attached Silicone Catheter and Tray. Indicated for central venous placement (either peripheral or chest placement) when patient therapy requires repeated venous access for injection or infusion therapy and/or venous blood sampling UPN: H787MPP5SAT0 Catalog Number: MP-P5SAT

Product Classification:

Class II

Date Initiated: September 20, 2022

Date Posted: November 2, 2022

Recall Number: Z-0132-2023

Event ID: 90924

Reason for Recall:

Printed Instructions for Use (IFU) not shipped with device. The Instructions for Use contain the Warnings, Precautions, Contraindications, and Procedures for the Preparation, Implantation, and Post Operative Care of the implantable port, failure to follow the Instructions for Use may result in patient injury.

Status: Ongoing

Product Quantity: 11 units

Code Information:

UDI-DI: 15051684018357 Lot Number: 5751582 Exp. Date: 31-Aug-2025

Distribution Pattern:

US Nationwide distribution in the states of AZ, CA, DC, IN, PA.

Voluntary or Mandated:

Voluntary: Firm initiated