PHILIPS MEDICAL SYSTEMS recalls
Every recall we track for PHILIPS MEDICAL SYSTEMS — 12 in all, from 2022–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from PHILIPS MEDICAL SYSTEMS peaked in 2025 (3); 12 since 2017.
All FDA recall records for PHILIPS MEDICAL SYSTEMS since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 2 | 0 | 2 |
| 2023 | 0 | 0 | 2 | 0 | 2 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 3 | 0 | 0 | 3 |
| 2026 (to date) | 0 | 0 | 5 | 0 | 5 |
What to do if you have a recalled PHILIPS MEDICAL SYSTEMS product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All PHILIPS MEDICAL SYSTEMS recalls
6 shown- Lower riskMedical device
PHILIPS MEDICAL SYSTEMS recalls Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model
Philips recalls Spectral CT 7500 RT systems with specific software versions and model numbers due to potential image artifacts and incorrect slice thickness. Affected units may require software updates to prevent safety issues.
PhilipsAug 21, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS recalls Brilliance iCT Brilliance iCT Upgrades Brilliance iCT SP Brilliance CT 64 Channel CT6000 Brilliance 64 Upgrades
Philips recalls certain CT scanners that may require manual triggering after Bolus Tracking scans, risking inadequate imaging and extra radiation exposure. Affected units may need rescan.
PhilipsJun 11, 2026 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS recalls Philips Spectral CT on Rails. Model Number: 728334.
Philips recalls Spectral CT on Rails model 728334 with software issues that may cause gantry to stay at scan position after pressing Go. Affected units have specific serial numbers and software versions.
PhilipsMar 7, 2026 - Use cautionMedical device
PHILIPS MEDICAL SYSTEMS recalls Model: Incisive CT for Brazil SKD; Product Code (REF): 728146; Software Versions: 5.1.0.X & 5.1.1.X;
Philips Medical Systems recalls Incisive CT software versions 5.1.0.X and 5.1.1.X for Brazil SKD models. Issues may cause incorrect scans, rescans, or missing ECG data. Affected units must be updated by software fix.
Philips Medical SystemsSep 25, 2025 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS recalls Spectral CT 7500: Software Version 5.0, Model 728333 and Spectral CT 7500 China: Software Version 5.0, Model 728340.
Philips recalls Spectral CT 7500 models with software version 5.0 due to potential misdiagnosis from incorrect image labeling. Affected units may require software update to prevent incorrect treatment.
PhilipsDec 13, 2023 - Lower riskMedical device
PHILIPS MEDICAL SYSTEMS recalls CombiDiagnost R90 1.1 (709031)
Philips recalls CombiDiagnost R90 1.1 (709031) models where RF viewer may display previous patient radiography images during fluoroscopy, causing image differences. Affected units have specific serial numbers.
PhilipsFeb 11, 2022
PHILIPS MEDICAL SYSTEMS recall questions
How many recalls has PHILIPS MEDICAL SYSTEMS had?
12 recalls from PHILIPS MEDICAL SYSTEMS are on record with U.S. safety agencies, from 2022–2026.
What is the most recent PHILIPS MEDICAL SYSTEMS recall?
PHILIPS MEDICAL SYSTEMS recalls Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model, dated Aug 21, 2026. Every PHILIPS MEDICAL SYSTEMS recall is listed on this page, newest first.
What should I do if I have a recalled PHILIPS MEDICAL SYSTEMS product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new PHILIPS MEDICAL SYSTEMS recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.