Quick Facts at a Glance
- Recall Date
- May 1, 2026
- Hazard Level
- HIGH
- Brand
- Philips North America
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Philips North America
- Model numbers
- Model Number: 712035. UDI: (01)00884838090705(21)24861049. Lot Code: 24861049.
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
May 1, 2026
Reported by FDA DEVICE
June 17, 2026
RecallRadar source check
June 23, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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 You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Philips North America Llc or your healthcare provider for instructions. Notification method: Letter
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Full Description
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.. Classification: Class II. Quantity: 1 unit. Distribution: US distribution to California.
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Safety Guide
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