FDA recall, , Moderate risk
Veritas Standard Glenoid Baseplate
The Veritas Standard Glenoid Baseplate has incorrect machining of a screw hole, potentially causing improper screw engagement.
Summary by Recall Canary from the FDA notice
What happened
restor3d Inc., of Durham, North Carolina, recalled the Veritas Standard Glenoid Baseplate, part of the Veritas Standard Reverse Total Shoulder system, because incorrect machining of the peripheral screw hole could result in improper engagement of the peripheral screws. The recall began June 30, 2026, and was added to the FDA's Enforcement Report on August 19, 2026. The product was distributed in Texas.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its model number and lot code are listed under that product.
Veritas Standard Glenoid Baseplate
- Model number
- 1500-1030
- 1500-1035
- Lot code
- A00030
- A00065
- A09828
- A09830
- A00064
- A09829
Recall details
- Company began the recall
- Sold in
U.S. Nationwide distribution in the state of Texas.
- Company
- restor3d Inc.Durham, North Carolina
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99402
- Recall number
- Z-2987-2026
All recalls from restor3d Inc.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
