Access Vascular, Inc: Medical Device Recall in 2023 - (Recall #: Z-1156-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (<30days) to the peripheral venous access system for intravenous therapy Product Number: 80004004

Product Classification:

Class II

Date Initiated: December 22, 2022

Date Posted: March 1, 2023

Recall Number: Z-1156-2023

Event ID: 91533

Reason for Recall:

Label with the incorrect component listed on the inner kit Tyvek header bag

Status: Ongoing

Product Quantity: 445 units

Code Information:

UDI-DI: (01)00850030354020 Lot Numbers: 11424032, 11432076

Distribution Pattern:

US Nationwide distribution in the states of CT, FL, NE, TN, TX, WA.

Voluntary or Mandated:

Voluntary: Firm initiated