Philips Healthcare recalls
Every recall we track for Philips Healthcare — 11 in all, from 2018–2023 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Philips Healthcare peaked in 2021 (5); 11 since 2017.
All FDA recall records for Philips Healthcare 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 | 4 | 0 | 4 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 5 | 0 | 5 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 1 | 0 | 1 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Philips Healthcare 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 Healthcare recalls
7 shown- Lower riskMedical device
Philips Healthcare recalls Incisive CT, software version 5.0
Philips Healthcare recalls Incisive CT software version 5.0 due to potential scan inaccuracies that could affect medical imaging results. Affected units may require software updates to ensure proper scan planning and safety.
Philips HealthcareAug 2, 2023 - Lower riskMedical device
Philips Healthcare recalls Philips StentBoost Live R2.0 application, when used with the Philips Azurion with software release R2.x
Philips recalls StentBoost Live R2.0 software for Azurion systems with R2.x software due to incorrect EPX database configuration causing acquisition to continue after 40 images instead of stopping automatically.
Philips HealthcareFeb 2, 2022 - Lower riskMedical device
Philips Healthcare recalls Philips Azurion systems with software releases 2.1(L1) and 2.1(L2)
Philips recalls Azurion systems with specific software versions due to potential 3D X-ray scan errors. Affected units may produce inaccurate scans if detector orientation is not precisely aligned.
Philips HealthcareSep 24, 2021 - Lower riskMedical device
Philips Healthcare recalls CombiDiagnost R90 is multi-functional general R/F systems.
Philips Healthcare recalls CombiDiagnost R90 medical devices due to missing required radiation labels, which could affect safety compliance. Affected units may need verification of labels.
Philips HealthcareSep 22, 2021 - Lower riskMedical device
Philips Healthcare recalls Azurion systems with software release R2.0.x
Philips Healthcare recalls Azurion systems with software release R2.0.x due to a defect causing incorrect patient type selection during studies, potentially affecting dose control. Affected units include Azurion R2.1 models.
Philips HealthcareMay 26, 2021 - Lower riskMedical device
Philips Healthcare recalls DigitalDiagnost C50, Stationary X-ray System
Philips recalls DigitalDiagnost C50 X-ray systems due to a missing label. This may affect safety and compliance. Contact Philips for details.
Philips HealthcareDec 21, 2018 - Lower riskMedical device
Philips Healthcare recalls Centron Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic,
Philips Healthcare recalls Centron imaging products for potential shutter reset during procedure changes, affecting vascular and cardiac imaging. Users should check model numbers and contact Philips for guidance.
Philips HealthcareJun 11, 2018
Philips Healthcare recall questions
How many recalls has Philips Healthcare had?
11 recalls from Philips Healthcare are on record with U.S. safety agencies, from 2018–2023.
What is the most recent Philips Healthcare recall?
Philips Healthcare recalls Incisive CT, software version 5.0, dated Aug 2, 2023. Every Philips Healthcare recall is listed on this page, newest first.
What should I do if I have a recalled Philips Healthcare 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 Healthcare 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.