Lower riskMedical device recall · FDA · Published May 19, 2023
Philips DigitalDiagnost C90 Software Login Issue: May Prevent User Access
Philips recalls DigitalDiagnost C90 models 712034 and 712035 due to a software login issue that may prevent user access. Affected units include specific serial numbers and UDI-DI codes.
“Philips DigitalDiagnost C90 Software Login Issue: May Prevent User Access.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/58154-philips-digitaldiagnost-c90-software-login-issue-may-prevent-user-access. Based on FDA recall #Z-2042-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2042-2023%22&limit=1).
Philips North America Llc recalled DigitalDiagnost C90 units due to a software login issue that may prevent users from logging in, according to the FDA. The agency announced the recall on May 19, 2023.
How to tell if you have it
DigitalDiagnost C90, Model No. 712034 and 712035
UPC 00884838090699
UPC 00884838090705
The hazard
The recall addresses a software login issue that may prevent the user from logging in, according to the FDA.
Context
GovInfoNow's records show Philips North America Llc has 129 other recalls on record since July 12, 2017. Other recent recalls of similar products include Philips Achieva 3.0T MRI Recalled: Software Issue May Terminate Scans (Aug. 21, 2026) and Philips Spectral CT 7500 Scanner May Cause Extra Radiation Exposure (Aug. 18, 2026). Additional recent recalls include Philips Brilliance CT 64 Medical Scanner Recall: Unintended Radiation Risk (Aug. 7, 2026) and GE Medical Systems Centricity Universal Viewer Software Cybersecurity Recall: Login Credentials at Risk (Jan. 30, 2026).
How to tell if you have this one
Check for model numbers 712034 or 712035 on the device. Affected units have specific serial numbers listed in the recall notice, including UDI-DI codes.
Brand
Philips
Product
DigitalDiagnost C90, Model No. 712034 and 712035
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Device Model
Identify the model number on your DigitalDiagnost C90 device to see if it is 712034 or 712035.
Verify Serial Number
Compare your device's serial number with the list of affected serial numbers provided in the recall notice.
Where it went and when
Where it was distributed
Distributed in 9 states, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “Distribution in US: AZ, GA, IN, IA, MN, NE, NH, OH, TX OUS distribution to Australia, Chile, China, Malta, Namibia, New Zealand, Oman, Panama, Qatar, Suriname, United Kingdom” States read from FDA’s own wording; “not listed” means the notice does not name it.
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-2042-2023 (May 19, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2042-2023 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.