Notice names this product. Philips North America’s DigitalDiagnost C90 Flex/Value/Chest/ER is named in FDA Class II recall Z-2354-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported hazard: 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. Identifying details: Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.. Units affected: 1 unit. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
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.
Company / brand: Philips North America recalls
Affected product: DigitalDiagnost C90 Flex/Value/Chest/ER recall status
Official ID Z-2354-2026 · Official record ↗
See all Philips North America recalls →
Found something wrong or missing? Report a data error.
Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.