restor3d Inc. recalls
Every recall we track for restor3d Inc. — 5 in all, from 2022–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from restor3d Inc. peaked in 2022 (3); 5 since 2017.
All FDA recall records for restor3d Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 2 | 1 | 3 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 2 | 0 | 2 |
What to do if you have a recalled restor3d Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All restor3d Inc. recalls
3 shown- Lower riskMedical device
restor3d Inc. recalls Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide), REF: 5831-9006
restor3d recalls Kinos Axiom Total Ankle Systems with incorrect patient-specific cutting guides that may cause delayed surgery, poor implant alignment, or revision surgery. Affected units have specific serial numbers and reference codes.
restor3dJul 27, 2026 - Lower riskMedical device
restor3d Inc. recalls Brand Name: Veritas Standard Reverse Total Shoulder Product Name: Veritas Standard Glenoid Baseplate Model/Catalog
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.
restor3dJun 30, 2026 - Lower riskMedical device
restor3d Inc. recalls Evans Wedge Disposable Trials, Medium Footprint, 10mm Thickness (6101-20181018). Orthopedic manual surgical instrument
restor3d recalls Evans Wedge Disposable Trials (6101-20181018) due to parts mixing during relabeling for 4-year shelf life. Affected units have specific model and lot numbers.
restor3dMar 30, 2022
restor3d Inc. recall questions
How many recalls has restor3d Inc. had?
5 recalls from restor3d Inc. are on record with U.S. safety agencies, from 2022–2026.
What is the most recent restor3d Inc. recall?
restor3d Inc. recalls Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide), REF: 5831-9006, dated Jul 27, 2026. Every restor3d Inc. recall is listed on this page, newest first.
What should I do if I have a recalled restor3d Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new restor3d Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.