News in brief: More info on Philips respiratory device recall; Expert recommendations on interstitial lung abnormalities; Call for Medicare review of procedural specialist incomes

More information on Philips respiratory device recall The TGA has provided additional advice on the Philips recall action for CPAP, Bi-Level PAP devices and mechanical ventilators. The regulator is urging users of the devices affected by the Urgent Product Defect Correction action to register them with the producer, though it acknowleges that Philips has been ...

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