# FDA recall Z-1987-2025

> **Preat Corp** · Class II · device recall initiated 2025-04-02.

## Product

Biomet 3i Certain-compatible 4.1 mm Milled Ti Abutment REF 9001767-F    Preat milled Abutments are intended to be used in conjunction with endosseous dental implants in the maxillary or mandibular arch to provide support for single-unit or multi-unit prosthetic restorations.

## Reason for recall

Due to manufacturing issues, abutment products were manufactured with screw seat located too high, which may cause the mating screw to have a shorter engagement length into the associated implant.

## Distribution

U.S. Nationwide distribution in the states of AZ, CA, GA, MO, NJ, NY, OH, PA, RI, TN,TX, and WA.

## Key facts

- **Recall number:** Z-1987-2025
- **Recalling firm:** Preat Corp
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-02
- **Report date:** 2025-06-25

- **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-1987-2025

## Citation

> AI Analytics. FDA recall Z-1987-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1987-2025. Source: US FDA. Licensed CC0.

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