# FDA recall Z-2107-2025

> **Preat Corp** · Class II · device recall initiated 2025-06-24.

## Product

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

## 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.

## Key facts

- **Recall number:** Z-2107-2025
- **Recalling firm:** Preat Corp
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-24
- **Report date:** 2025-07-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Santa Maria, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2107-2025

## Citation

> AI Analytics. FDA recall Z-2107-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2107-2025. Source: US FDA. Licensed CC0.

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