Lower riskMedical device recall · FDA · Published June 30, 2021
GE Healthcare Revolution Apex CT Scanners: Incorrect Dose Display Risk
GE Healthcare recalls Revolution Apex and Revolution CT with Apex Edition scanners due to potential inaccurate radiation dose displays, which could lead to unnecessary radiation exposure during scans.
The accumulated dose is incorrectly displayed in certain situations. There are two situations that will result in the SmartStep displayed dose being inaccurately high.
Take action
Contact the company
📍Recalling firmGE Healthcare, LLC3000 N Grandview Blvd · Waukesha, WI 53188-1615
“GE Healthcare Revolution Apex CT Scanners: Incorrect Dose Display Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62259-ge-healthcare-revolution-apex-ct-scanners-incorrect-dose-display-risk. Based on FDA recall #Z-0815-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0815-2022%22&limit=1).
The FDA announced on June 30, 2021, that GE Healthcare LLC is recalling Revolution Apex and Revolution CT with Apex Edition devices because the accumulated dose may be incorrectly displayed as inaccurately high. This Class II recall affects 273 units distributed worldwide.
How to tell if you have it
GE Healthcare Revolution Apex
GE Healthcare Revolution CT with Apex Edition
The hazard
The device displays an incorrectly high SmartStep dose in certain situations. The FDA stated there are two specific situations that result in this inaccurate reading.
Context
GovInfoNow's records show GE Healthcare LLC has 97 other recalls on record since Oct. 4, 2017. Other recent recalls of similar products include GE Healthcare SIGNA Premier MRI Scanners (Feb. 27, 2026), GE Centricity Universal Viewer 6.0/7.0/8.0 (July 15, 2022), and GE Healthcare SIGNA Premier MRI Scanner Recall (June 24, 2022). Other recent recalls of similar products include Philips Ingenuity CT Scanners (Aug. 7, 2026), GE Healthcare Revolution Apex Elite CT Scanners (March 26, 2026), and Philips Brilliance CT 64 Medical Scanner Recall (Aug. 7, 2026).
How to tell if you have this one
Check if your scanner model is Revolution Apex or Revolution CT with Apex Edition. These models were sold by GE Healthcare starting in 2019.
Brand
GE Healthcare
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.
Classification
Class II
Status
Ongoing
Distribution
Worldwide - US Nationwide distribution.
Recall number
Product, codes & lots
Quantity
Z-0815-2022
Revolution Apex, Revolution CT with Apex Edition; Revolution Apex, Revolution CT with Apex Edition
273 (51 US, 222 OUS) in total
Z-0816-2022
Revolution CT, Revolution CT ES; Revolution CT, Revolution CT ES
273 (51 US; 222 OUS) in total
Based on the official FDA remedy
What to do — step by step
Check Scanner Model
Identify your scanner model by checking the label on the device or the software settings.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide - US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 9 months 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-0815-2022 (June 30, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0815-2022 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.