FDA Device recall Z-2354-2026
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035
- FDA Device
- Class II
- ongoing
- Published 2026-06-17
On 2026-06-17 the FDA classified a Class II recall of DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035 by Philips North America, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2354-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-05-01 |
| Published | 2026-06-17 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Philips North America |
| Distribution | CA |
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.
Identifiers
| code_info | Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Other recalls by Philips North America
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FDA Device · Class II · 2026-10-07 · Philips North America - MR 7700
FDA Device · Class II · 2026-10-07 · Philips North America - SmartPath to MR 7700
FDA Device · Class II · 2026-10-07 · Philips North America - Upgrade to MR 7700
FDA Device · Class II · 2026-10-07 · Philips North America - Upgrade dStream
FDA Device · Class II · 2026-10-07 · Philips North America
All Philips North America recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2354-2026%22
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