Access Vascular, Inc: Medical Device Recall in 2023 - (Recall #: Z-1605-2023)

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:

HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004

Product Classification:

Class II

Date Initiated: March 3, 2023

Date Posted: May 24, 2023

Recall Number: Z-1605-2023

Event ID: 92124

Reason for Recall:

The catheter packaged with specific lots of the HydroPICC Kits and HydroMID Kits have a shorter expiration date than what is listed on the outer kit package.

Status: Ongoing

Product Quantity: 240 units

Code Information:

UDI-DI: 00862559000487; Lot Number: 11423949

Distribution Pattern:

US distribution to States of: FL, TN, TX.

Voluntary or Mandated:

Voluntary: Firm initiated