Access Vascular, Inc recalls HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002

Recalled February 22, 2023 · FDA recall Z-1129-2023 · Access Vascular

Hazard

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. · FDA Class II

Units

1,789 HydroMID devices

Sold at

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

Description

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.

Product

HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002

Manufacturer(s)

Access Vascular, Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →