IntelliVue Multi Measurement Server — Class II medical device recall Z-0292-2018
Ongoing recall by Philips Electronics North America Corporation, reported 2018-01-03, distributed nationwide. Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips IntelliVue Patient Monitors
| Recall number | Z-0292-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Electronics North America Corporation, Andover, MA, United States |
| Recall initiated | 2017-08-23 |
| Classified | 2017-12-27 |
| Reported by FDA | 2018-01-03 |
| Distributed | Nationwide (US) |
| Quantity | 7,071 |
| Model numbers | 862442, M3002A, M300IA/AL, M8102A, M8105A, MP2, MP5 |
Product
IntelliVue Multi Measurement Server, IntelliVue Multi Measurement Server SLCP, IntelliVue Multi Measurement Server X2, IntelliVue Patient Monitor Models MP2 and MP5 Product Usage: Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Intended for monitoring, recording, and alarming of multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment.
Reason for recall
Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips IntelliVue Patient Monitors
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-0292-2018. 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.