FDA DeviceClass IINotable
FDA Recall: Philips Avalon Fetal Monitor, FM 30 Part numberM2703A
Description
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
Hazard
Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or permanent loss of speaker output.
Remedy
169 units
Related Recalls
2026-07-01 · FDA_DEVICE
FDA Recall: Philips Avalon Fetal Monitor, FM20, Part number M2702A, Part M2703A
Philips North America Llc
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
2026-06-17 · FDA_DEVICE
FDA Recall: DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Philips North America Llc