FDA Device recall Z-1671-2025
WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments
- FDA Device
- Class II
- ongoing
- Published 2025-04-30
On 2025-04-30 the FDA classified a Class II recall of WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments by Straumann Usa, citing incorrect blister labelling.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1671-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-04-17 |
| Published | 2025-04-30 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Straumann Usa |
| Distribution | US |
Product
WB XL Anatomic Healing Abutment XC. Endosseous Dental Implant Abutments.
Reason
Incorrect blister labelling.
Identifiers
| code_info | Article No. 064.4522S and 064.4523S; UDI (01)07630031775856(11)240613(17)290612(10)GNNA2, (01)07630031775856(11)241115(…Article No. 064.4522S and 064.4523S; UDI (01)07630031775856(11)240613(17)290612(10)GNNA2, (01)07630031775856(11)241115(17)291114(10)JZYZ3, (01)07630031775856(11)241216(17)291215(10)KRJA6, (01)07630031775863(11)240604(17)290603(10)GJXT4, (01)07630031775863(11)241011(17)291010(10)JLLP9, (01)07630031775863(11)241120(17)291119(10)KCKL1, (01)07630031775863(11)241211(17)291210(10)KPRE4, (01)07630031775863(11)250219(17)300218(10)LWZM6; Lot No. (Expiration Date): GNNA2 (6/12/29), JZYZ3 (11/14/29), KRJA6 (12/15/29), GJXT4 (6/3/29), JLLP9 (10/10/29), KCKL1 (11/19/29), KPRE4 (12/10/29), and LWZM6 (2/18/30). |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1671-2025%22
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