# FDA recall Z-2354-2026

> **Philips North America Llc** · Class II · device recall initiated 2026-05-01.

## Product

DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.

## Reason for recall

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.

## Distribution

US distribution to California.

## Key facts

- **Recall number:** Z-2354-2026
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-01
- **Report date:** 2026-06-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cambridge, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2354-2026

## Citation

> MORVS. FDA recall Z-2354-2026. Retrieved 2026-10-21 from https://api.morvs.ai/recall/Z-2354-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*