FDA recall Z-0857-2019

Philips North America, LLC · Class II · device

Product

PageWriter TC70 w/trolley Government Bundle, Product 860352, Software revisions up to and including A.07.05. 22 to evaluate the electrocardiogram of adult and pediatric patients

Reason for recall

Philips PageWriter TC cardiograph batteries which have reached end of life may overheat, causing the case to melt and/or the device to ignite, which can cause injury to patient or nearby users.

Distribution

Domestic distribution nationwide. Foreign distribution worldwide.

Key facts

Status
Ongoing
Initiation date
2019-01-09
Report date
2019-02-27
Voluntary/Mandated
Voluntary: Firm initiated
Location
Andover, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0857-2019