FDA recall, , Moderate risk
Philips Smart-Hopping 2.0 AP 1.4 GHz
Philips Smart-hopping 2.0 AP 1.4 GHz has unreliable wireless roaming behavior that can cause loss of connectivity to the central monitoring system.
Summary by Recall Canary from the FDA notice
What happened
Philips North America initiated a recall of the Philips Smart-hopping 2.0 AP 1.4 GHz, model number 867216, on September 16, 2026, due to unreliable wireless roaming behavior of Smart-hopping 1.0 wireless clients during transport when connecting to Smart-hopping 2.0 infrastructure, which can result in loss of connectivity to the central monitoring system (PIC iX). The recall was added to the FDA's Enforcement Report and classified on October 16, 2026, with US Nationwide distribution.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its model number matches.
Product/
- Model
- 867216
Recall details
- Company began the recall
- Sold in
US Nationwide distribution.
- Company
- Philips North America
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99908
- Recall number
- Z-0199-2027
All recalls from Philips North America
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
