# FDA recall Z-1995-2026

> **Straumann USA LLC** · Class II · device recall initiated 2026-03-27.

## Product

Straumann n!ce Zr, HT, Full-arch Restoration. Article 010.0158.    Endosseous Dental Implant Abutments

## Reason for recall

Includes an incorrect screw seat interface.

## Distribution

US distribution to AL, AZ, FL, HI, LA, MD, OH, VA.

## Key facts

- **Recall number:** Z-1995-2026
- **Recalling firm:** Straumann USA LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-27
- **Report date:** 2026-05-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Andover, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1995-2026

## Citation

> AI Analytics. FDA recall Z-1995-2026. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1995-2026. Source: US FDA. Licensed CC0.

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