Philips North America Llc recalls Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.
- Recall date
- December 12, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1033-2026
- FDA classification
- Class II
- Brand / firm
- Philips North America Llc
- Sold / distributed
- US Nationwide distribution.
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor.
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