Philips North America Llc
4
Recalls
0
Units Recalled
0
Injuries
0
Deaths
Categories: Medical Device
2026-06-17 to 2026-07-01
| Date | Source | Product | Brand | Severity | Units |
|---|---|---|---|---|---|
| 2026-07-01 | FDA Device | FDA Recall: Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A | Philips North America Llc | Class II | N/A |
| 2026-07-01 | FDA Device | FDA Recall: Philips Avalon Fetal Monitor, FM 30 Part numberM2703A | Philips North America Llc | Class II | N/A |
| 2026-07-01 | FDA Device | FDA Recall: Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following system descript | Philips North America Llc | Class II | N/A |
| 2026-06-17 | FDA Device | FDA Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035. | Philips North America Llc | Class II | N/A |