---
title: "DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. — FDA record Z-2354-2026 | Is It on Recall"
description: "System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during"
url: https://isitonrecall.com/recall/fda-device-z-2354-2026-digitaldiagnost-c90-flex-value-chest-er-model-number-712035/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. — FDA record Z-2354-2026

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 1, 2026. 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**: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
- **Reason**: System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.
- **Classification**: Class II
- **Recalling firm**: Philips North America Llc
- **Quantity**: 1 unit
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2354-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2354-2026%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 | Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049. |

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

## Distribution

US distribution to California.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [California](https://isitonrecall.com/state/california/)

## Dates in the source

- **Report date**: Jun 17, 2026
- **Recall initiation date**: May 1, 2026
- **Center classification date**: Jun 5, 2026

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-2354-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Philips North America Llc records](https://isitonrecall.com/brand/philips-north-america-llc/)