Philips Healthcare (Suzhou) Co., Ltd. recalls
Every recall we track for Philips Healthcare (Suzhou) Co., Ltd. — 4 in all, from 2021–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for Philips Healthcare (Suzhou) Co., Ltd. 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 | 1 | 0 | 0 | 1 |
| 2022 | 0 | 0 | 1 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 1 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 1 | 0 | 1 |
What to do if you have a recalled Philips Healthcare (Suzhou) Co., Ltd. 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 (Suzhou) Co., Ltd. recalls
4 shown- Lower riskMedical device
Philips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144.
Philips Healthcare recalls specific Incisive CT models with software V4.5 and V5.0 due to potential failure to trigger clinical scans during bolus tracking. Affected units have product codes 728143 or 728144.
Philips HealthcareJun 26, 2026 - Lower riskMedical device
Philips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT
Philips Healthcare recalls Incisive CT devices due to unstable sensor connections that may cause incomplete scans. Affected units were sold in China. Consumers should contact Philips for details.
Philips HealthcareDec 3, 2025 - Lower riskMedical device
Philips Healthcare (Suzhou) Co., Ltd. recalls Incisive CT, model 728143 & 728144 running Software Version 5.0.0.
Philips Healthcare recalls Incisive CT models 728143 & 728144 with software version 5.0.0 due to potential misdiagnosis from image artifacts and incorrect labels. Affected units may require rescan or correction.
Philips HealthcareDec 23, 2022 - Use cautionMedical device
Philips Healthcare (Suzhou) Co., Ltd. recalls Philips CT systems are advanced continuous-rotation computed tomography systems suitable for a wide range of computed
Philips Healthcare recalls CT systems with Incisive CT couch that may fail to self-lock, causing unexpected downward movement. Affected units have specific Unique Device Identifiers.
Philips HealthcareFeb 24, 2021
Philips Healthcare (Suzhou) Co., Ltd. recall questions
How many recalls has Philips Healthcare (Suzhou) Co., Ltd. had?
4 recalls from Philips Healthcare (Suzhou) Co., Ltd. are on record with U.S. safety agencies, from 2021–2026.
What is the most recent Philips Healthcare (Suzhou) Co., Ltd. recall?
Philips Healthcare (Suzhou) Co., Ltd. recalls Philips Incisive CT with software V4.5&V5.0, Product Code 728143 and Product Code 728144., dated Jun 26, 2026. Every Philips Healthcare (Suzhou) Co., Ltd. recall is listed on this page, newest first.
What should I do if I have a recalled Philips Healthcare (Suzhou) Co., Ltd. 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 (Suzhou) Co., Ltd. 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.