---
title: "3D Systems VSP Reconstruction, Model: VSPR-301 Product: Scapula Marking Guide... — FDA record Z-1510-2022 | Is It on Recall"
description: "Scapula Marking Guide (anatomically Shaped) was incorrectly designed."
url: https://isitonrecall.com/recall/fda-device-z-1510-2022-3d-systems-vsp-reconstruction-model-vspr-301-product-scapula-marking-guide-anatomically-shaped-rx-on/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# 3D Systems VSP Reconstruction, Model: VSPR-301 Product: Scapula Marking Guide (Anatomically Shaped), Rx Only, Non-Ste... — FDA record Z-1510-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 17, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 3D Systems VSP Reconstruction, Model: VSPR-301 Product: Scapula Marking Guide (Anatomically Shaped), Rx Only, Non-Sterile
- **Reason**: Scapula Marking Guide (anatomically Shaped) was incorrectly designed.
- **Classification**: Class II
- **Recalling firm**: Medical Modeling, Inc.
- **Quantity**: 1 unit
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-1510-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1510-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot # 167559; UDI: (01) 00816847020886 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

International distribution in the country of Germany.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Aug 17, 2022
- **Recall initiation date**: May 17, 2022
- **Center classification date**: Aug 9, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1510-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medical Modeling, Inc. records](https://isitonrecall.com/brand/medical-modeling-inc/)