FDA Says Philips Filed 21,000 Reports on Bad Foam Aug-Oct

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The FDA on Wednesday said Philips filed 21,000 medical device reports in connection with faulty foam in its ventilation and sleep apnoea devices in the Aug-Oct 2022 period.
Reuters Health Information

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FDA Says Philips Filed 21,000 Reports on Bad Foam Aug-Oct

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Medscape FDA Says Philips Filed 21,000 Reports on Bad Foam Aug-Oct The FDA on Wednesday said Philips filed 21,000 medical device reports in connection with faulty foam in its ventilation and sleep apnoea devices in the Aug-Oct 2022 period.Reuters Health Information

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