Philips North America Llc
1
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-06-17 to 2026-06-17
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-06-17 | FDA Device | FDA Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. | Philips North America Llc | Class II | N/A |