Philips North America recalls

Philips North America appears in 532 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.

• IntelliVue MX40 Patient Monitor, Product number 865352, Service Numbers All: 453564262571, 453564262591, 453564615311, 453564615331, 453564…
  FDA Device · Class II · 2019-06-12 · Philips North America
• IntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers All other countries: 453564451791, 453564451811, 453564467721, 4535…
  FDA Device · Class II · 2019-06-12 · Philips North America
• IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All: 453564711531 and 453564711541 - Product Usage: Used primarily…
  FDA Device · Class II · 2019-06-12 · Philips North America
• IntelliVue MX40 Patient Monitor, Product number 865350, Service # USA: 453564262491 and 453564262511 - Product Usage: Used primarily as a t…
  FDA Device · Class II · 2019-06-12 · Philips North America
• SureSigns VS3 NBP, SpO2, Product Number 863071
  FDA Device · Class II · 2019-05-22 · Philips North America
• SureSigns VS3 NBP, SpO2, Rec, Product Number 863072
  FDA Device · Class II · 2019-05-22 · Philips North America
• SureSigns VS3 NBP, SpO2, Temp, Rec, Product Number 863074
  FDA Device · Class II · 2019-05-22 · Philips North America
• SureSigns VS4 Government Bundle, Product Number 863286
  FDA Device · Class II · 2019-05-22 · Philips North America
• SureSigns VS3 NBP, Product Number 863069
  FDA Device · Class II · 2019-05-22 · Philips North America
• SureSigns VS3 NBP, SpO2, Temp, Product Number 863073
  FDA Device · Class II · 2019-05-22 · Philips North America
• SureSigns VS3 NBP Temp, Product Number 863070
  FDA Device · Class II · 2019-05-22 · Philips North America
• SureSigns VS4 NBP, SpO2, Product Number 863283
  FDA Device · Class II · 2019-05-22 · Philips North America
• Fetal Spiral Electrode, Model No. 9898 031 37631
  FDA Device · Class II · 2019-05-08 · Philips North America
• Azurion FlexArm, 722079
  FDA Device · Class II · 2019-04-17 · Philips North America
• Urodiagnost, Product No. 708033 Product Usage: The Philips UroDiagnost MRF can be used to perform all urological and gynecological routine…
  FDA Device · Class II · 2019-04-03 · Philips North America
• MultiDiagnost Eleva w/ Flat Detector, Product codes 708034, 708037, 708038 Product Usage: As a multifunctional I universal imaging applicat…
  FDA Device · Class II · 2019-04-03 · Philips North America
• URODiagnost Eleva, Product codes 708026, 708027, 708028 Product Usage: The Philips OmniDiagnost is a multi-functional, universal X-ray syst…
  FDA Device · Class II · 2019-04-03 · Philips North America
• Lithium-ion Rechargeable Batteries for the Philips MX40 Wearable Monitor REF: 989803176201 - Product Usage: Indicated for use by health car…
  FDA Device · Class II · 2019-04-03 · Philips North America
• MultiDiagnost-Eleva, Product codes 708032, 708036 Product Usage: As a multifunctional I universal imaging application system, General RIF,…
  FDA Device · Class II · 2019-04-03 · Philips North America
• 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