# FDA recall Z-1275-2025

> **Hiossen Inc.** · Class II · device recall initiated 2025-01-27.

## Product

ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures.  Model/Catalog Number: ETRGA4524MP

## Reason for recall

Patient chart stickers provided inside the packaging may incorrectly identify ET Rigid Abutments as Regular version whereas the actual product is a Mini version; and identify the ET Multi Abutments as Mini version whereas the actual product is a Regular version

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1275-2025
- **Recalling firm:** Hiossen Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-27
- **Report date:** 2025-03-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Fairless Hills, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1275-2025

## Citation

> AI Analytics. FDA recall Z-1275-2025. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1275-2025. Source: US FDA. Licensed CC0.

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