Use cautionMedical device recall · FDA · Published October 21, 2021
Philips CombiDiagnost R90 1.0/1.1 Systems Recall: Overvoltage Risk of Fire
Philips recalls CombiDiagnost R90 1.0 and 1.1 multi-functional systems (model 709030/709031) due to overvoltage causing electrical fire risk. Affected units may show smoke, popping sounds, or fire in the cabinet.
If the system experiences an overvoltage / power surge it can cause a short circuit condition within the Main- cabinet. If this issue occurs, the user may experience an electrical fire within the cabinet, see or smell smoke emitting from the cabinet, or hear a popping sound coming from the cabinet.
Take action
Contact the company
📍Recalling firmPhilips North America Llc222 Jacobs St · Cambridge, MA 02141-2289
✎ GovInfoNow plain-language explainer
Philips is recalling CombiDiagnost R90 1.0 and 1.1 multi-functional systems (model numbers 709030 and 709031) because electrical overvoltage can cause short circuits and fire in the cabinet. This poses a risk of fire, smoke, or popping sounds if the system experiences a power surge. Read more at govinfonow.com/recall/61640-philips-combidiagnost-r90-1-0-1-1-systems-recall-overvoltage.
“Philips CombiDiagnost R90 1.0/1.1 Systems Recall: Overvoltage Risk of Fire.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61640-philips-combidiagnost-r90-1-0-1-1-systems-recall-overvoltage. Based on FDA recall #Z-1355-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1355-2023%22&limit=1).
The FDA announced on Oct. 21, 2021, that Philips North America LLC is recalling CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F systems due to a potential electrical fire hazard. Owners should contact the company for remedies. The recall affects 512 units distributed nationwide and globally.
How to tell if you have it
Brand: Philips
Product: CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system
Model Numbers: 709030, 709031
UPCs: 00884838076747, 00884838101456
The hazard
If the system experiences an overvoltage or power surge, it can cause a short circuit within the Main-cabinet. This may result in an electrical fire, smoke emitting from the cabinet, or a popping sound coming from the cabinet.
Context
GovInfoNow's records show Philips North America LLC has issued 129 other recalls since July 12, 2017. Recent recalls include Ingenia systems with software issues terminating examinations (Aug. 21, 2026) and Spectral CT scanners risking extra radiation exposure (Aug. 18, 2026). Other recent recalls of similar products include Allura Xper FD10C Medical System Recall: Risk of Electrical Short-Circuits (Dec. 15, 2025) and Allura Xper FD10F Medical System Recall: Risk of Electrical Short-Circuits (Dec. 15, 2025).
How to tell if you have this one
Check for model numbers 709030 or 709031 on the product label. The system may also have serial numbers starting with 10000000 through 10000199 or higher as listed in the recall notice.
Brand
Philips
Product
CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 709030 and 709031
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
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-1355-2023 (October 21, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1355-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.