WB XL Anatomic Healing Abutment XC — Class II medical device recall Z-1671-2025
Ongoing recall by Straumann USA LLC, reported 2025-04-30, distributed nationwide. Incorrect blister labelling.
| Recall number | Z-1671-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Straumann USA LLC, Andover, MA, United States |
| Recall initiated | 2025-04-17 |
| Classified | 2025-04-24 |
| Reported by FDA | 2025-04-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | BE, CA, CN, NL, SE |
| Quantity | 1,786 units |
| UPC / GTIN / UDI-DI | 07630031775856, 07630031775863 |
| Lot numbers | GJXT4, GNNA2, JLLP9, JZYZ3, KCKL1, KPRE4, KRJA6, LWZM6 |
Product
WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments.
Reason for recall
Incorrect blister labelling.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1671-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.