DigitalDiagnost C90 Flex/Value/Chest/ER recall
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Why was DigitalDiagnost C90 Flex/Value/Chest/ER recalled?
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 should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
- Product
- DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
- Recalling firm
- Philips North America Llc
- Quantity
- 1 unit
- Distribution
- US distribution to California.
- Recall date
- June 17, 2026
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)