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

Recall Z-2895-2018 — Philips SureSigns VM 3/4/6/8 Patient Monitors, 863063 863064 863065 863066 863068 863077 863085 863086 863317 863287 863288 863289 The SureSigns VM4, VM6, and VM8 patient monitors are for use by health care professionals whenever there is a need for monitoring the physiological parame

U.S. FDA — Device Enforcement · United States · 2018-07-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2895-2018
Date of alert
2018-07-13
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)
00884838028791
Reported risk: Philips has received several reports in which monitors with lithium ion batteries that had exceeded their battery life expectancy have overheated or ignited. These batteries should be replaced every 3 years or upon reaching 300 charge-discharge cycles. Although the Philips SureSigns VS & VM Monitors and View Station (VSV) can display actual information on either or both battery age and charge-discharge cycles, the existing labeling does not include full instructions on how to use this information to determine when to replace the battery. An overheated battery may in turn cause the device case to overheat and possibly melt or cause the device to ignite, which can cause injury to a patient, nearby users, or cause damage to property.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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