3D Systems VSP Reconstruction — Class II medical device recall Z-1510-2022
Ongoing recall by Medical Modeling, Inc., reported 2022-08-17. Scapula Marking Guide (anatomically Shaped) was incorrectly designed.
| Recall number | Z-1510-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Modeling, Inc., Littleton, CO, United States |
| Recall initiated | 2022-05-17 |
| Classified | 2022-08-09 |
| Reported by FDA | 2022-08-17 |
| Countries outside the US | DE |
| Quantity | 1 units |
| UPC / GTIN / UDI-DI | 00816847020886 |
| Lot numbers | 167559 |
| Model numbers | VSPR-301 |
Product
3D Systems VSP Reconstruction, Model: VSPR-301 Product: Scapula Marking Guide (Anatomically Shaped), Rx Only, Non-Sterile
Reason for recall
Scapula Marking Guide (anatomically Shaped) was incorrectly designed.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1510-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.