DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. recall (Philips North America Llc)
Medical deviceClass IIOngoing
Summary: Philips North America Llc is recalling 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.
What is being recalled
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Why
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.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US distribution to California. (states named: California)
How to tell if yours is affected
Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-2354-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | May 1, 2026 |
| Reported | June 17, 2026 |
| Company | Philips North America Llc |
| Company location | Cambridge, MA, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 1 unit |
More recalls from Philips North America Llc · all medical device recalls · recalls from May 2026