FDA Device recall Z-0686-2025

Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216

• FDA Device
• Class II
• ongoing
• Published 2024-12-25

On 2024-12-25 the FDA classified a Class II recall of Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216 by Philips North America, citing 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 potenti….

Read the official FDA Device notice

Product

Philips Smart-Hopping 2.0 AP 1.4 GHz. Model Number: 867216

Reason

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 client device to appear to drop out from the network. 2. if the Access Point experiences a disconnection from the Access Point Controller exceeding 4 minutes, the Access Point may not transition through the desired state to all for clean reconnection of the client radio link. 3. Potential to experience higher than expected data dropouts, device disassociations/reassociations for their wireless clients, and frequent "Loss of AP" alerts. 4. Potential for the Smart-hopping Access Point is affected by a software issue where the Access Point will resent after 82.85 days when the frame counter reaches its limit. This causes the latest synchronization check to fail and potential for loss of patient data.

Identifiers

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0686-2025%22

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