DigitalDiagnost C90 recallZ-2354-2026 · Philips North America Llc · initiated May 1, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Philips North America Llc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was 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.
FDA root cause category: Device Design
What the company is doing
Philips Medical notified the single consignee on about 05/01/2026 via mailed letter. The consignee was notified of the issue, potential risk, and instructed to Stop using the Wall Stand VS2 immediately to ensure patient and user safety while Philips provides the Seismic Bucky Unit 2 (BU2) Skyplate kit, do not attempt to inspect, adjust, or install any mechanical components of the Wall Stand yourself, circulate this Urgent Medical Device Correction letter to all users of this device so that they are aware of the issue and associated impact, and complete and return the provided response form. A Philips representative will contact the consignee to schedule a time for a Field Service Engineer (FSE) to visit the site to install a hardware correction.
Recall details
- Recall number
- Z-2354-2026
- Status
- Open, Classified
- Initiated by the company
- May 1, 2026
- Posted by the FDA
- Jun 5, 2026
- Recalling firm
- Philips North America Llc
- Quantity
- 1 unit
- Product code
- MQB
- FDA submissions
- K202564
- Distribution
- US distribution to California.
Product description
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Code information (models, lots, serial numbers)
Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- DigitalDiagnost C90 712035Philips Medical Systems DMC GmbH · Solid state x-ray imager (flat panel/digital imager)4 recalls17 reports
Product lines
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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