# FDA recall Z-1671-2025

> **Straumann USA LLC** · Class II · device recall initiated 2025-04-17.

## Product

WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments.

## Reason for recall

Incorrect blister labelling.

## Distribution

Worldwide distribution - US Nationwide and the countries of Belgium, Canada, China, Netherlands, and Sweden.

## Key facts

- **Recall number:** Z-1671-2025
- **Recalling firm:** Straumann USA LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-17
- **Report date:** 2025-04-30

- **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-1671-2025

## Citation

> AI Analytics. FDA recall Z-1671-2025. Retrieved 2026-07-12 from https://api.ai-analytics.org/recall/Z-1671-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*