Some 70 incident reports potentially related to the affected machines were received by the Health Products Regulatory Authority.

Medical device company Philips announced a recall of millions of sleep apnea machines and ventilators because a material used inside them could put users at risk of cancer or other health issues.

This article originally appeared on ProPublica. The Food and Drug Administration rarely uses its authority to pull dangerous medical devices off the market and is so poorly staffed that it’s sometimes ...

PITTSBURGH — A Pennsylvania federal court remanded a California woman’s negligence complaint over injuries allegedly caused by a recalled Philips CPAP device back to Los Angeles County Superior Court.