Class II

Medical Device Recall: WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments.

Straumann USA LLC · April 17, 2025

Reason for Recall

Incorrect blister labelling.

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

1,786 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1671-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.