# FDA recall Z-2318-2024

> **Preat Corp** · Class II · device recall initiated 2024-04-10.

## Product

9006767 Astra EV 4.8mm Milled Titanium Abutment    Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.

## Reason for recall

Due to incorrect milled titanium abutment being packaged and labeled.

## Distribution

U.S.: CA, MO, and NV.  O.U.S.: None

## Key facts

- **Recall number:** Z-2318-2024
- **Recalling firm:** Preat Corp
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-10
- **Report date:** 2024-07-17

- **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-2318-2024

## Citation

> AI Analytics. FDA recall Z-2318-2024. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-2318-2024. Source: US FDA. Licensed CC0.

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