Philips North America Llc: Device Recall
Recall #Z-1033-2026 · 12/12/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1033-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Philips North America Llc
- Status
- Ongoing
- Date Initiated
- 12/12/2025
- Location
- Cambridge, MA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 13,470 Units
Reason for Recall
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.
Product Description
Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.
Distribution Pattern
US Nationwide distribution.
Other Recalls by Philips North America Llc
- Class II: Risk 10/31/2025
- Class II: Risk 10/31/2025
- Class II: Risk 10/31/2025
- Class II: Risk 10/31/2025
- Class II: Risk 10/31/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.