Philips North America recalls
Philips North America appears in 563 official U.S. recall notices indexed by RecallRadar.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- Omnidiagnost Classic, Product Codes 70859, 708023, 708024, 708025 Product Usage: The Philips OmniDiagnost is a multi-functional, universal…
FDA Device · Class II · 2019-04-03 · Philips North America - PageWriter TC50 Government Bundle, Product 860429, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of a…
FDA Device · Class II · 2019-02-27 · Philips North America - PageWriter TC70, Product 860315, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pedi…
FDA Device · Class II · 2019-02-27 · Philips North America - PageWriter TC30, Product 860306, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric…
FDA Device · Class II · 2019-02-27 · Philips North America - PageWriter TC30 w/o trolley Government Bundle, Product 860355, Software revisions up to and including A.07.05.22 to evaluate the electrocar…
FDA Device · Class II · 2019-02-27 · Philips North America - PageWriter TC50, Product 860310, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pedi…
FDA Device · Class II · 2019-02-27 · Philips North America - PageWriter TC70 w/trolley Government Bundle, Product 860352, Software revisions up to and including A.07.05. 22 to evaluate the electrocard…
FDA Device · Class II · 2019-02-27 · Philips North America - PageWriter TC30 w/ trolley Government Bundle, Product 860354, Software revisions up to and including A.07.05.22 to evaluate the electrocard…
FDA Device · Class II · 2019-02-27 · Philips North America - PageWriter TC70 w/o trolley Government Bundle, Product 860353, Software revisions up to and including A.07.05.22 to evaluate the electrocar…
FDA Device · Class II · 2019-02-27 · Philips North America - PageWriter TC20, Product 860332, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric…
FDA Device · Class II · 2019-02-27 · Philips North America - HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx Monitor/Defibrillators
FDA Device · Class II · 2018-12-19 · Philips North America - MRx Defibrillator Model # M3535A & M3536A, UDI 00884838000018(21)US00601969 Product Usage: The HeartStart MRx is for use for the terminatio…
FDA Device · Class I · 2018-02-14 · Philips North America - HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536…
FDA Device · Class I · 2017-04-05 · Philips North America