Veritas Standard Glenoid Baseplate
restor3d recalls Veritas Standard Glenoid Baseplate over screw hole machining defect.
If you have a Veritas Standard Glenoid Baseplate, stop using it and contact restor3d Inc. for instructions on returning the affected component.
Why it was recalled
restor3d Inc. is recalling the Veritas Standard Glenoid Baseplate, a component of the Reverse Total Shoulder Arthroplasty System, due to incorrect machining of the peripheral screw hole, which may result in improper engagement of the peripheral screws. The patient-specific baseplate is not affected.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
Veritas Standard Reverse Total Shoulder Veritas Standard Glenoid BaseplateUDI-DI: 00840097513225, 00840097513232Model/Catalog number: 1500-1030, 1500-1035Software version: N/A - off-the-shelf hardware product
| Lot code |
|---|
| – |
| 1500-1030, A00030, A00065, A09828, A09830, 1500-1035, A00064, A09829 |
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other Device Defect recalls
Editorial summary by Recall Canary · summary updated 2026-08-21 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification