Philips Smart-hopping 2.0 Ap 1.4 Ghz. Patient Monitor.
Recall Summary Philips is recalling the Smart-hopping 2.0 AP 1.4 GHz Patient Monitor (MX40 device) because it may fail to reconnect to network access points when moving between locations if the wireless signal strength changes rapidly. This could affect hospitals and healthcare facilities using this monitoring system. The recall is classified as Class II, indicating a potential serious health consequence.
- Recalling firm
- Philips North America Llc
- Product
- Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.
- Reason
- It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength changed quickly.
- Classification
- Class II
- Category
- consumer product recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2025-12-12
- Status
- Open, Classified
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/724b38d5-c294-47e7-8155-6d75c14d909a