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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Monitoring Devices

Philips Smart-Hopping 2.0 Access Points Recalled for Connection and Data Risks

Agency Publication Date: December 17, 2024
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Summary

Philips North America has recalled approximately 4,811 units of the Philips Smart-Hopping 2.0 Access Point (Model 867216). These wireless network devices, used in hospitals and medical facilities, are experiencing software issues that can cause them to fail to connect, drop data during patient roaming, or automatically reset every 82 days when a internal counter reaches its limit. These devices were distributed nationwide and sold directly to hospitals and authorized medical distributors. No injuries or incidents of data loss have been reported to date.

Risk

The software defects can cause a sudden loss of network connection or frequent alerts, which may lead to the loss of real-time patient monitoring data or delays in critical medical alerts reaching healthcare providers.

What You Should Do

  1. The recalled products are Philips Smart-Hopping 2.0 AP 1.4 GHz wireless access points, Model Number 867216, across all software versions.
  2. To determine if your network infrastructure is affected, check the model number and Unique Device Identifier (UDI) labels on the access point units. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  4. For additional information, you can contact the FDA at 1-888-463-6332.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Philips Smart-Hopping 2.0 AP 1.4 GHz
Model / REF:
867216
Serial Numbers (141):
(01)00884838099876(21)DK34706344
(01)00884838099876(21)DK33603995
(01)00884838099876(21)DK34706512
(01)00884838099876(21)DK33402245
(01)00884838099876(21)DK34706012
(01)00884838099876(21)DK33402324
(01)00884838099876(21)DK33603538
(01)00884838099876(21)DK34405346
(01)00884838099876(21)DK32801033
(01)00884838099876(21)DK34705955
(01)00884838099876(21)DK40307155
(01)00884838099876(21)DK34405363
(01)00884838099876(21)DK33604046
(01)00884838099876(21)DK34706011
(01)00884838099876(21)DK34706010
(01)00884838099876(21)DK33402486
(01)00884838099876(21)DK34405820
(01)00884838099876(21)DK34405539
(01)00884838099876(21)DK34405788
(01)00884838099876(21)DK33403107
(01)00884838099876(21)DK33603456
(01)00884838099876(21)DK34706099
(01)00884838099876(21)DK32801250
(01)00884838099876(21)DK32801095
(01)00884838099876(21)DK33604249
(01)00884838099876(21)DK33403062
(01)00884838099876(21)DK34706432
(01)00884838099876(21)DK33403214
(01)00884838099876(21)DK33402554
(01)00884838099876(21)DK40307129
(01)00884838099876(21)DK33603678
(01)00884838099876(21)DK32801039
(01)00884838099876(21)DK33402660
(01)00884838099876(21)DK34706048
(01)00884838099876(21)DK33904683
(01)00884838099876(21)DK33402439
(01)00884838099876(21)DK34405702
(01)00884838099876(21)DK40306709
(01)00884838099876(21)DK32800996
(01)00884838099876(21)DK34405910
(01)00884838099876(21)DK32800867
(01)00884838099876(21)DK33603918
(01)00884838099876(21)DK33604048
(01)00884838099876(21)DK33904818
(01)00884838099876(21)DK34706539
(01)00884838099876(21)DK34405884
(01)00884838099876(21)DK33403219
(01)00884838099876(21)DK33603727
(01)00884838099876(21)DK34706371
(01)00884838099876(21)DK33402675
UDI:
00884838099876
GTIN:
00884838099876

All software versions are affected. Hardware features an internal frame counter that triggers a reset after 82.85 days of operation.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95847
Status: Active
Manufacturer: Philips North America Llc
Sold By: Direct to hospitals; Authorized medical distributors
Manufactured In: United States
Units Affected: 4,811 units
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.