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.
Take action
Contact the company
📍Recalling firmPhilips North America Llc222 Jacobs St · Cambridge, MA 02141-2289
“Philips DigitalDiagnost C90 Flex/Value/Chest/ER Recall: Seismic Stability Risk.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/49256-philips-digitaldiagnost-c90-flex-value-chest-er-recall-seismic-stability. Based on FDA recall #Z-2354-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2354-2026%22&limit=1).
The FDA announced on May 1, 2026, that Philips North America Llc is recalling one DigitalDiagnost C90 Flex/Value/Chest/ER unit (model 712035) because it was delivered without the required Seismic kit for the Wall Stand VS2. The agency said this omission could prevent the stand from remaining stable during seismic events.
How to tell if you have it
Brand: Philips
Product: DigitalDiagnost C90 Flex/Value/Chest/ER
Model Number: 712035
UPC: 00884838090705
Lot Code: 24861049
Distribution: California
The hazard
According to the FDA, the system was delivered without the required Seismic kit for Wall Stand VS2. The agency stated this kit is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.
Context
GovInfoNow's records show Philips North America Llc has issued 129 other recalls since July 12, 2017. Recent Philips recalls include an August 21, 2026, recall of Ingenia 3.0T models due to software issues terminating examinations and an August 18, 2026, recall of Spectral CT 7500 systems where the Bolus tracking scan application may crash. Other recent recalls of similar products include a January 26, 2026, Philips Azurion 7 B20 System Recall for unexpected table movement risk and December 10, 2025, GE Maxxus and SMV BodyTrack Nuclear Medicine Systems Recalls citing risks of detector fall injury.
How to tell if you have this one
Check for model number 712035 on the device. The product was sold in the U.S. with lot code 24861049.
Brand
Philips
Product
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Wall Stand Stability
Ensure the wall stand has the seismic kit installed before use during earthquakes.
Where it went and when
Where it was distributed
Distributed in California.
Listed by the agency
Not listed
FDA distribution: “US distribution to California.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California.
Recall timeline
FDA published this recall 47 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2354-2026 (May 1, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2354-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.