Philips Ultrasound, Inc
90 FDA enforcement actions
90 Total Recalls
0 Class I
21 Class II
69 Class III
Firm Details
- Product Types
- device
- States
- PA
All Recalls
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class III: Low Risk 07/03/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
- Class II: Risk 05/28/2025 device
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.