Philips DigitalDiagnost C90 Flex/Value/Chest/ER recalled for missing seismic stabilization kit
One Philips DigitalDiagnost C90 Flex/Value/Chest/ER X-ray system was shipped without the required Seismic kit for its Wall Stand VS2. The kit is designed to keep the stand stable and prevent damage during earthquakes or seismic events.
From the FDA notice · Read the official notice ↗ · All Philips recalls
What to do
- If you operate a Philips DigitalDiagnost C90 with model number 712035, contact Philips to obtain the missing Seismic kit for the Wall Stand VS2.
- Do not use the Wall Stand VS2 in an earthquake-prone area until the seismic kit is installed.
Is yours affected?
Compare your label or packaging with the recalled product.
- Product
- DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
- Sold in
- US distribution to California.
- Made for
- All ages (0 months and older)
Details
- Units affected
- 1 unit
- Illnesses reported
- None reported
- Manufactured in
- 222 Jacobs St, N/A, Cambridge, MA, United States
- Classification
- Class II
- Recall number
- Z-2354-2026
In the FDA's words
- Description
- DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. 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. Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049. Distribution: US distribution to California. Affected quantity: 1 unit
- 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.
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