Access Vascular, Inc: Medical Device Recall in 2023 - (Recall #: Z-1129-2023)

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 - Basic Kit, Model Number 80004002

Product Classification:

Class II

Date Initiated: December 16, 2022

Date Posted: February 22, 2023

Recall Number: Z-1129-2023

Event ID: 91426

Reason for Recall:

Select catheter lots were identified to be labeled with incorrect expiration date, where the catheters expire prior to the labeled expiration date of the kit.

Status: Ongoing

Product Quantity: 1,789 HydroMID devices

Code Information:

UDI-DI: (01)00850030354006; Lot Number: 11428361, 11393260, 11395226

Distribution Pattern:

US Nationwide distribution in the states of CT, IL, IN, MA, NE, TN, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated