By Anthony O. Goriainoff

 

Koninklijke Philips NV said Thursday that test results of the volatile organic compounds emissions of the first-generation DreamStation devices show that exposure to the VOC's identified so far isn't anticipated to result in long-term health consequences for patients.

The Dutch health-technology group said that its overall guidance for physicians and patients in June's recall notification was unchanged at this time.

On June 14, the company's subsidiary, Philips Respironics, issued a voluntary recall notification for certain sleep and respiratory care products to address potential health risks related to the polyester-based polyurethane sound abatement foam in these devices.

Philips said it has conducted a comprehensive test and research program on the foam to assess the potential patient health risks related to possible emission of particulates from degraded foam and certain VOCs.

"Comprehensive particulate testing and analyses are now expected to be completed in the second quarter of 2022, as testing protocols in compliance with the full extent of the relevant ISO standards for all affected product platforms require long lead times of multiple months," the company said.

 

Write to Anthony O. Goriainoff at anthony.orunagoriainoff@dowjones.com

 

(END) Dow Jones Newswires

December 23, 2021 02:37 ET (07:37 GMT)

Copyright (c) 2021 Dow Jones & Company, Inc.
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