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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 9 of 9 Results
Related Medical Device Recalls
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Product Description
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Z-0856-2019 - PageWriter TC20, Product 860332, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients 2 02/21/2019 Philips North America, LLC
Z-0859-2019 - 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 2 02/21/2019 Philips North America, LLC
Z-0861-2019 - 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 2 02/21/2019 Philips North America, LLC
Z-0855-2019 - PageWriter TC30, Product 860306, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients 2 02/21/2019 Philips North America, LLC
Z-0860-2019 - 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 2 02/21/2019 Philips North America, LLC
Z-0854-2019 - PageWriter TC50, Product 860310, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pediatric patients 2 02/21/2019 Philips North America, LLC
Z-0858-2019 - 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 2 02/21/2019 Philips North America, LLC
Z-0857-2019 - 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 2 02/21/2019 Philips North America, LLC
Z-0853-2019 - PageWriter TC70, Product 860315, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pediatric patients 2 02/21/2019 Philips North America, LLC
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