Drug recall
Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216
FDA recall event 95847 · Class II · Philips North America Llc
Key facts
| Event ID | 95847 |
|---|---|
| Recall numbers | Z-0686-2025 |
| Recalling firm | Philips North America Llc |
| Product type | Devices |
| Products | Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The following four issues are included: 1. Certain Channel Settings may result in an Access Point preventing a connected client device from roaming to another Access Point potentially causing the… |
| Initiation date | Nov 20, 2024 |
| Report date | Dec 25, 2024 |
| City | Cambridge |
| State | MA |
| Country | United States |
| FEI number | 3016618143 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: