Philips Respironics, Inc.
17 FDA enforcement actions
17 Total Recalls
16 Class I
1 Class II
0 Class III
Firm Details
- Product Types
- device
- States
- PA
All Recalls
- Class II: Risk 10/07/2025 device
- Class I: Dangerous 06/30/2025 device
- Class I: Dangerous 06/30/2025 device
- Class I: Dangerous 06/30/2025 device
- Class I: Dangerous 05/09/2025 device
- Class I: Dangerous 05/09/2025 device
- Class I: Dangerous 05/09/2025 device
- Class I: Dangerous 10/07/2024 device
- Class I: Dangerous 10/07/2024 device
- Class I: Dangerous 10/07/2024 device
- Class I: Dangerous 10/07/2024 device
- Class I: Dangerous 10/07/2024 device
- Class I: Dangerous 10/07/2024 device
- Class I: Dangerous 10/07/2024 device
- Class I: Dangerous 07/16/2024 device
- Class I: Dangerous 07/16/2024 device
- Class I: Dangerous 07/16/2024 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.