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Lower risk Medical device recall · FDA · Published October 5, 2017

Philips Network Firewall (Cisco ASA 5506) may lose connection to Information Center after

Philips recalls Network Firewall (Cisco ASA 5506) Model #867098 that may stop working after 18+ months of use, causing Information Center iX to reboot. Affected units have specific serial numbers listed.

🇺🇸 FDA recall #Z-0850-2018Medical devicePhilips ›
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Recalling firmPhilips Electronics North America Corporation3000 Minuteman Rd · Andover, MA 01810-1032
✎ GovInfoNow plain-language explainer

What happened, in plain English

Philips is recalling Network Firewalls (Cisco ASA 5506) with model number 867098 that may stop working after more than 18 months of use. This could cause the Information Center iX or Classic to reboot unexpectedly, disrupting medical device connections. Read more at govinfonow.com/recall/72903-philips-network-firewall-cisco-asa-5506-may-lose-connection-to.

Source Summary by GovInfoNow · govinfonow.com/recall/72903-philips-network-firewall-cisco-asa-5506-may-lose-connection-to · Updated September 17, 2026 · FDA enforcement record: FDA #Z-0850-2018

Cite this page

“Philips Network Firewall (Cisco ASA 5506) may lose connection to Information Center after.” GovInfoNow, updated September 17, 2026. https://govinfonow.com/recall/72903-philips-network-firewall-cisco-asa-5506-may-lose-connection-to. Based on FDA recall #Z-0850-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0850-2018%22&limit=1).

Why it’s dangerous

The firewall contains a clock signal component that has a high probability of failing after 18+ months of use. When this component fails, the firewall stops working and cannot be recovered, causing communication loss between medical devices. This may trigger the Information Center to reboot.

Who’s affected

Healthcare providers using Philips Information Center iX or Classic medical monitoring systems with the recalled Network Firewall. Patients using these systems may experience temporary disruption in monitoring.

How to tell if you have this one

Check if your Network Firewall has model number 867098 and serial numbers starting with JMX2030Y2 or JMX2035Y0. These units were sold with Philips IntelliVue Information Center iX or Classic.

  • Brand
    Philips
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Model Number

    Look for model number 867098 on the firewall's label.

  2. Verify Serial Number

    Check if your serial number starts with JMX2030Y2 or JMX2035Y0.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “US Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 21 months after the firm started it.

1. Firm started the recall: Oct 5, 201712. FDA classified it Class II: Mar 2, 201823. Published in FDA’s Enforcement Report: Mar 14, 201834. FDA terminated the recall: Jul 1, 2019420172019
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-0850-2018 (October 5, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0850-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on September 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA