FDA says Philips filed 21,000 reports on bad foam Aug-Oct.
FDA says Philips filed 21,000 reports on bad foam Aug-Oct.,The U.S. Food and Drug Administration (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.

FDA says Philips filed 21,000 reports on bad foam Aug-Oct.

The U.S. Food and Drug Administration (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.