The Metrix Company recalls Imed Products Imed EVA BAG, 150 mL, 2-PORTS, REF IM38040; An empty single-use pouch made of plastic intended to contain…

Recall date

October 9, 2024

Source

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

Recall number

Z-0342-2025

FDA classification

Class II

Brand / firm

The Metrix Company

Sold / distributed

Worldwide - US Nationwide distribution in the states of TX, IL, OH, PA, WA, MD, IL, UT, CA, MA, PA, MI, FL, PR, and the country of Canada.

Why it was recalled

A limited number of IV bags have been found to leak during filling.

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

What was recalled

Imed Products Imed EVA BAG, 150 mL, 2-PORTS, REF IM38040; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.