Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0292-2017 — Philips IntelliVue MX40 Patient Monitor: IntelliVue MX40 Smart-hopping (2.4GHz) Product Number: 865351 Worldwide Except USA Exchange part: 453564262491 453564262511 453564615311 453564615331 453564262571 453564262591 Exchange part: 453564262531 453564262551 453564262571 4535642625

U.S. FDA — Device Enforcement · United States · 2016-09-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0292-2017
Date of alert
2016-09-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips Electronics North America Corporation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
453564262491
Reported risk: Philips IntelliVue MX40 Patient Wearable Monitor Configuration Setting Disables Generation and Delivery of ECG Alarms to PIIC iX
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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