The Recall Desk

Manufacturer

Philips North America, LLC

410 recalls in our database name Philips North America, LLC as the manufacturing or recalling firm.

What the numbers show

Total
410
Critical
2
Severe
26
Most recent
2026-09-09

Of the 410 recalls from Philips North America, LLC we have scored against our rubric, 2 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 26 (6%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

401–410 of 410

  • SevereFDA (Devices)·Z-0861-2019·2019-02-27

    Philips PageWriter TC30 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling PageWriter TC30 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing injury risks to patients and users.

    Product
    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
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0854-2019·2019-02-27

    Philips PageWriter TC50 ECG Devices Recalled for Overheating and Fire Risk

    Philips is recalling PageWriter TC50 electrocardiogram devices because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC50, Product 860310, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0855-2019·2019-02-27

    Philips PageWriter TC30 ECG Devices Recalled for Overheating and Ignition Risk

    Philips is recalling PageWriter TC30 ECG devices because end-of-life batteries may overheat, melt the case, or ignite, posing injury risks to patients and users.

    Product
    PageWriter TC30, Product 860306, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0857-2019·2019-02-27

    Philips PageWriter TC70 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling 57 PageWriter TC70 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing a risk of injury to patients and users.

    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
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0859-2019·2019-02-27

    Philips PageWriter TC30 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling PageWriter TC30 cardiographs because end-of-life batteries may overheat, melt, or ignite, posing injury risks to patients and users.

    Product
    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
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0856-2019·2019-02-27

    Philips PageWriter TC20 Recall for Battery Overheating and Fire Risk

    Philips is recalling PageWriter TC20 devices because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury.

    Product
    PageWriter TC20, Product 860332, Software revisions up to and including A.07.05.22 to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0853-2019·2019-02-27

    Philips PageWriter TC70 Cardiograph Recall for Battery Overheating Risk

    Philips is recalling PageWriter TC70 cardiographs because end-of-life batteries may overheat, melt the case, or ignite, posing a risk of injury to patients and users.

    Product
    PageWriter TC70, Product 860315, Software revisions up to and including A.07.05.22 used to evaluate the electrocardiogram of adult and pediatric patients
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0603-2019·2018-12-19

    Philips Recalls HeartStart MRx Lithium-Ion Batteries Due to Defective Component

    Philips is recalling 1,880 HeartStart MRx lithium-ion batteries because a defective component may prevent the battery from charging or delivering power to the monitor/defibrillator.

    Product
    HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx Monitor/Defibrillators.
    Category
    Medical Device
    Distribution
    32 states
  • HighFDA (Devices)·Z-0489-2018·2018-02-14

    Philips HeartStart MRx Defibrillators Recalled for Defective Component

    Philips is recalling 71 HeartStart MRx defibrillators because a defective component may prevent shock delivery in AED mode.

    Product
    MRx Defibrillator Model # M3535A & M3536A, UDI 00884838000018(21)US00601969 Product Usage: The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-1417-2017·2017-04-05

    Philips HeartStart MRx Monitor/Defibrillator Recalled for Potential Failure to Deliver Therapy

    Philips is recalling HeartStart MRx Monitor/Defibrillators because they may fail to deliver therapy or monitoring when operating on a single battery.

    Product
    HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9
    Category
    Medical Device
    Distribution
    Distributed nationwide