Class II

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

Preat Corp · June 24, 2025

Reason for Recall

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

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

44 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2107-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Preat Corp Medical Device Recall: Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only | SafeCheck