Philips North America, LLC - SureSigns VS4 Government Bundle - Class 2 Recall
SureSigns VS4 Government Bundle, Product Number 863286. For monitoring the physiological parameters of patients (NBP, SpO2 & Temperature). (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 14, 2019 Category: Medical Devices Source Type: alerts
Philips North America, LLC - PageWriter TC30 w/ trolley Government Bundle - Class 2 Recall
PageWriter TC30 w/ trolley Government Bundle, Product 860354, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 22, 2019 Category: Medical Devices Source Type: alerts
Philips North America, LLC - PageWriter - Class 2 Recall
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 (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 22, 2019 Category: Medical Devices Source Type: alerts
Philips North America, LLC - PageWriter TC30 with out trolley Government Bundle - Class 2 Recall
PageWriter TC30 w/o trolley Government Bundle, Product 860355, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 22, 2019 Category: Medical Devices Source Type: alerts
Philips North America, LLC - PageWriter TC50 Government Bundle - Class 2 Recall
PageWriter TC50 Government Bundle, Product 860429, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 22, 2019 Category: Medical Devices Source Type: alerts
Philips North America, LLC - PageWriter TC70 w/o trolley Government Bundle - Class 2 Recall
PageWriter TC70 w/o trolley Government Bundle, Product 860353, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients (Source: Medical Device Recalls)
Source: Medical Device Recalls - February 22, 2019 Category: Medical Devices Source Type: alerts
