---
title: "Symbia Intevo Bold and Symbia Intevo 6 SPECT/CT Systems — FDA record Z-0893-2022 | Is It on Recall"
description: "There is a quality issue with the three bolts that hold the CT balancing weights, which could create a safety issue."
url: https://isitonrecall.com/recall/fda-device-z-0893-2022-symbia-intevo-bold-and-symbia-intevo-6-spect-ct-systems/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Symbia Intevo Bold and Symbia Intevo 6 SPECT/CT Systems — FDA record Z-0893-2022

Reported terminated

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 Mar 11, 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**: Symbia Intevo Bold and Symbia Intevo 6 SPECT/CT Systems
- **Reason**: There is a quality issue with the three bolts that hold the CT balancing weights, which could create a safety issue.
- **Classification**: Class II
- **Recalling firm**: Siemens Medical Solutions USA, Inc.
- **Quantity**: 7 devices
- **Agency-reported status**: Terminated
- **Source record identifier**: Z-0893-2022

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0893-2022%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 | A) Symbia Intevo Bold system; Model Number 11007962; Serial Numbers: 1) 1499 (UDI:40568690011591499) 2) 1501(UDI: 40568690011591501) 3) 1505 (UDI: 40568690011591505) 4) 1510 (UDI: 40568690011591510) B) Symbia Intevo 6 system; Model Number 10764803; Serial Numbers: 1) 2352 (UDI: 40568690012342352) 2) 2353 (UDI: 40568690012342353) 3) 2354 (UDI: 40568690012342354) |

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

## Distribution

Distribution OUS only to El Salvador, France, Germany, Japan, Taiwan, and UK.

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

## Dates in the source

- **Report date**: Apr 13, 2022
- **Recall initiation date**: Mar 11, 2022
- **Center classification date**: Apr 7, 2022
- **Termination date**: Apr 14, 2023

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-0893-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Siemens Medical Solutions USA, Inc records](https://isitonrecall.com/brand/siemens-medical-solutions-usa-inc/)