Philips North America: Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms)
Recall Summary Philips is recalling certain patient physiological monitors (model 867216) with arrhythmia detection that use Smart-hopping 1.0 wireless technology. These monitors can lose their wireless connection to the central monitoring system when moved between locations while connected to newer Smart-hopping 2.0 infrastructure. This recall affects units distributed nationwide across all U.S. states and Washington, D.C.
- Recalling firm
- Philips North America
- Product
- Philips Smart-hopping 2.0 AP 1.4 GHz; Product/Model Number: 867216;
- Reason
- Unreliable wireless roaming behavior of Smart-hopping 1.0 wireless clients during transport when connecting to Smart-hopping 2.0 infrastructure, resulting in loss of connectivity to the central monitoring system (PIC iX).
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-09-16
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d987ead2-46ea-4427-b957-0970a9f89975