Official recall notice
FDA DeviceClass IINotable
FDA Recall: Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplat
- Recall date
- 2026-08-26
- Brand
- restor3d Inc.
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.
Product description
Due to incorrect machining of peripheral screw hole resulting in potential for improper engagement of the peripheral screws.
Affected products
Lot Code: Model No 1500-1030; UDI-DI 00840097513225; Lot Numbers A00030, A00065, A09828, A09830 Model No 1500-1035; UDI-DI 00840097513232; Lot Numbers A00064, A09829