Access Vascular, Inc: Medical Device Recall in 2023 - (Recall #: Z-1155-2023)

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 Model Number: 80004004

Product Classification:

Class II

Date Initiated: December 22, 2022

Date Posted: March 1, 2023

Recall Number: Z-1155-2023

Event ID: 91529

Reason for Recall:

Product Mislabeled on the outer bag and inner kit Tyvek header bag

Status: Ongoing

Product Quantity: 155 units

Code Information:

UDI: (01)00850030354020 Lot Number: 11434018

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated