Lower riskMedical device recall · FDA · Published June 30, 2026
restor3d Veritas Standard Glenoid Baseplate Recall: Improper Screw Engagement Risk
restor3d recalls Veritas Standard Glenoid Baseplate models 1500-1030 and 1500-1035 due to potential improper screw engagement. Affected patients should contact the manufacturer for details.
“restor3d Veritas Standard Glenoid Baseplate Recall: Improper Screw Engagement Risk.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/697960-restor3d-veritas-standard-glenoid-baseplate-recall-improper-screw-engagement-risk. Based on FDA recall #Z-2987-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2987-2026%22&limit=1).
restor3d Inc. recalled Veritas Standard Glenoid Baseplates due to incorrect machining of peripheral screw holes that may prevent proper screw engagement, according to the FDA on June 30, 2026.
How to tell if you have it
Brand: Veritas Standard Reverse Total Shoulder
Product Name: Veritas Standard Glenoid Baseplate
Model/Catalog Number: 1500-1030; 1500-1035
Lot Numbers A00030, A00065, A09828, A09830 (Model No 1500-1030)
Lot Numbers A00064, A09829 (Model No 1500-1035)
UDI-DI 00840097513225
UDI-DI 00840097513232
The hazard
The recall involves potential for improper engagement of the peripheral screws due to incorrect machining of a peripheral screw hole, according to the FDA.
Context
GovInfoNow's records show restor3d Inc. has two other recalls on record since March 30, 2022. Other recent recalls of similar products include Tornier Perip Screw Recall (Dec. 19, 2025), Howmedica Triathlon Baseplate Size 3 Recall (May 19, 2026), and Waldemar Link Endo-Model Replacement Plateau Recall (Jan. 12, 2026).
How to tell if you have this one
Check for model numbers 1500-1030 or 1500-1035 on the baseplate. The product was sold as part of the restor3d Reverse Total Shoulder Arthroplasty System.
Brand
restor3d
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Contact Manufacturer
Reach out to restor3d Inc. for specific instructions on how to handle the recalled baseplate.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “U.S. Nationwide distribution in the state of Texas.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 57 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2987-2026 (June 30, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2987-2026 to see it in context.
Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.