In connection with a June 2021 Philips products recall, our law firm is investigating possible lawsuits against Philips for patients who have developed cancer or experienced organ failure following toxic exposures from the polyester-based polyurethane (PE-PUR) sound abatement foam component in these recalled Philips products:
Philips Bi-Level Positive Airway Pressure (Bi-Level PAP) Devices
Philips Continuous Positive Airway Pressure (CPAP) Devices
Philips Mechanical Ventilators
In more detail, there was a June 2021 Philips products recall for certain Philips Bi-Level PAP devices, Philips CPAP devices, and Philips Mechanical Ventilators due to possible toxic exposures from the polyester-based polyurethane (PE-PUR) sound abatement foam component in those Philips products.
From our perspective, the most serious possible resulting medical conditions for patients who used one of the recalled Philips Bi-Level PAP devices, Philips CPAP devices, or Philips Mechanical Ventilators are:
Cancers, such as:
— Lung Cancer
— Liver Cancer
— Kidney Cancer
Organ Failures, such as:
— Liver Failure
— Kidney Failure
In this document (accessed 6/24/2021), “Medical Device recall notification (U.S. only) / field safety notice (International Markets)“, from Philips Respironics, there is some product identification information about the various Philips Bi-Level PAP devices, Philips CPAP devices, and Philips Mechanical Ventilators affected by this June 2021 Philips products recall — as well as what Philips products are not affected by this recall, and why.
If you or someone you know used one of the recalled Philips Bi-Level PAP devices, Philips CPAP devices, or Philips Mechanical Ventilators and, in turn, developed cancer or experienced organ failure, we are providing free case evaluations for possible lawsuits against Philips. You can use our online Philips Breathing Devices Case Evaluation Form or, if you prefer, call us on our toll-free number, 800-426-9535.
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