Philips Cisco 3850 layer 3 switch — Class II medical device recall Z-1106-2017
Terminated recall by Philips Electronics North America Corporation, reported 2017-02-01, distributed in AK, CA, CO, FL, GA, KY, NC, NE…. May experience a loss of centralized monitoring.
| Recall number | Z-1106-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Electronics North America Corporation, Andover, MA, United States |
| Recall initiated | 2016-12-27 |
| Classified | 2017-01-26 |
| Reported by FDA | 2017-02-01 |
| Terminated | 2020-10-08 |
| Distributed | AK, CA, CO, FL, GA, KY, NC, NE, NH, NJ, NY, OH, PA, SC, TN, TX, VA, WA, WV |
| Countries outside the US | CA, DE, GB, JP, NZ, PL |
| Quantity | 107 |
| Model numbers | WS-C3850-12S-E |
Product
Philips Cisco 3850 layer 3 switch, 865339 model WS-C3850-12S-E in use with IntelliVue Information Center iX or Classic Information Center
Reason for recall
May experience a loss of centralized monitoring.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1106-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.