DigitalDiagnost C90 Flex/Value/Chest/ER — Class II medical device recall Z-2354-2026
Ongoing recall by Philips North America Llc, reported 2026-06-17, distributed in CA. System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage
| Recall number | Z-2354-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America Llc, Cambridge, MA, United States |
| Recall initiated | 2026-05-01 |
| Classified | 2026-06-05 |
| Reported by FDA | 2026-06-17 |
| Distributed | CA |
| Quantity | 1 units |
| Reason classes | specification failure |
| UPC / GTIN / UDI-DI | 00884838090705 |
| Lot numbers | 24861049 |
| Model numbers | 712035 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2354-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.