Preat Corp recalls Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only

Recall date

June 24, 2025

Source

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

Recall number

Z-2107-2025

FDA classification

Class II

Brand / firm

Preat Corp

Sold / distributed

US Nationwide distribution in the states of AL, CA, FL, GA, KY, MD, MN, NY, OK, PA.

Why it was recalled

Due to manufacturing error, digital analog rotational feature is 180 degrees off.

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

What was recalled

Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only