Philips Consumer Lifestyle
FDA Regulatory Profile
Philips Consumer Lifestyle appears in FDA public data with 1 recall, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0689-2018, Class II) was initiated on February 2, 2018. Its most recent 510(k) clearance was granted on September 3, 2026.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| Z-0689-2018 | Class II | Philips Avent Smart Ear Thermometer (SCH740), Philips Ear Thermometer (DL8740) | February 2, 2018 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K261622 | Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model: SCF593/52, SCF593/62); P | September 3, 2026 |
| K253754 | Philips Lumea IPL | December 23, 2025 |
| K243453 | Philips Lumea IPL | February 10, 2025 |
| K151033 | Philips Self-Adhesive Electrodes | July 28, 2015 |
| K151035 | PulseRelief | July 21, 2015 |