Access Vascular, Inc recalls HydroPICC 4Fr Single Lumen Catheter, Maximal Barrier Kit, Model Number 80001004

Recall date

March 3, 2023

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1605-2023

FDA classification

Class II

Brand / firm

Access Vascular, Inc

Sold / distributed

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

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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